Log in

Relevant bibliographies by topics / Benzimidazol / Journal articles

To see the other types of publications on this topic, follow the link: Benzimidazol.

Journal articles on the topic 'Benzimidazol'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Benzimidazol.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Krishnamurthy, Naik, and Narashimaiah Shashikala. "Synthesis of ruthenium(II) carbonyl complexes with 2-monosubstituted and 1,2-disubstituted benzimidazoles." Journal of the Serbian Chemical Society 74, no. 10 (2009): 1085–96. http://dx.doi.org/10.2298/jsc0910085k.

Full text

Abstract:

The reaction of the polymeric carbonyl complex [RuCl2(CO)2]x with 2-monosubstituted and 1,2-disubstituted benzimidazoles and 1,4-bis(benzimidazol- 2-yl)benzene (L9) in 2-methoxyethanol produces various coloured complexes of the formulae [Ru(CO)2Cl2(L)2]?xH2O (L = 1-(o-hydroxybenzyl)-2-(o-hydroxyphenyl)benzimidazole (L1), 1-(o-hydroxyphenyl)benzimidazole (L4), 1-(p-hydroxyphenyl)benzimidazole (L5), 1-(p-chlorobenzyl)-2-p-chlorophenyl) benzimidazole (L7), 1-[1-(dimethylamino)benzyl]-2-[1-(dimethylamino) phenyl]benzimidazole (L10), x = 0; L = 2-benzylbenzimidazole (L8), 1,4-bis(benzimidazol-2-yl)

APA, Harvard, Vancouver, ISO, and other styles

2

Sawant, Ramesh, and Deepali Kawade. "Synthesis and biological evaluation of some novel 2-phenyl benzimidazole-1-acetamide derivatives as potential anthelmintic agents." Acta Pharmaceutica 61, no. 3 (2011): 353–61. http://dx.doi.org/10.2478/v10007-011-0029-z.

Full text

Abstract:

Synthesis and biological evaluation of some novel 2-phenyl benzimidazole-1-acetamide derivatives as potential anthelmintic agentsThe present study describes synthesis of a series of 2-phenyl benzimidazole-1-acetamide derivatives and their evaluation for anthelmintic activity using Indian adult earthworms,Pheretima posthuma.The structure of the title compounds was elucidated by elemental analysis and spectral data. The compounds 4-({[2-(4-nitrophenyl)-1H-benzimidazol-1-yl]acetyl}amino) benzoic acid (3a),N-ethyl-2-[2-(4-nitrophenyl)-1H-benzimidazol-1-yl] acetamide (3c),N-benzyl-2-[2-(4-nitrophen

APA, Harvard, Vancouver, ISO, and other styles

3

Al-Warhi, Tarfah, Mohamed Said, Mahmoud El Hassab, et al. "Unexpected Synthesis, Single-Crystal X-ray Structure, Anticancer Activity, and Molecular Docking Studies of Certain 2–((Imidazole/Benzimidazol–2–yl)thio)–1–arylethanones." Crystals 10, no. 6 (2020): 446. http://dx.doi.org/10.3390/cryst10060446.

Full text

Abstract:

In connection with our research program concerning development of novel effective benzimidazole-based anticancer candidates, herein we describe a new unexpected synthetic route to obtain a series of 2–((imidazole/benzimidazol2–yl)thio)1–arylethanones endowed with promising anti-breast cancer and Cyclin-dependent kinase 2 (CDK2) inhibitory activities. Contrary to expectations, products for the reaction of 2–mercaptoimidazole/benzimidazole 2a,b with β–keto esters 6a–c were unambiguously assigned as 2–((imidazol/benzimidazol2–yl)thio)1–arylethanones 10a–f based on NMR spectroscopy and single-crys

APA, Harvard, Vancouver, ISO, and other styles

4

Borovskoy, Valery A., Sergey A. Komykhov, Vladimir I. Musatov, Svetlana V. Shishkina, Oleg V. Shishkin, and Sergey M. Desenko. "Unusual reaction of 2-(aminomethyl)benzimidazole with chalcones: Synthesis of new aryl-substituted pyrrolines." Collection of Czechoslovak Chemical Communications 74, no. 9 (2009): 1403–10. http://dx.doi.org/10.1135/cccc2009018.

Full text

Abstract:

The reaction of 2-(aminomethyl)benzimidazole (1) with chalcones 2a–2e leads to formation of 3,5-diaryl-2-benzimidazol-2-yl-4,5-dihydropyrroles 3a–3e. The trans orientation of benzimidazol-2-yl and 3-aryl substituents in 3a–3e was established by X-ray analysis of 3e.

APA, Harvard, Vancouver, ISO, and other styles

5

Ahmadi, Abbas, and Babak Nahri-Niknafs. "Synthesis, Characterization of Some Novel Benzimidazole Derivatives of 1-Bromo-2,4-dinitrobenzene and Their Antifungal Activities." E-Journal of Chemistry 8, s1 (2011): S85—S90. http://dx.doi.org/10.1155/2011/685246.

Full text

Abstract:

Six novel benzimidazole derivatives, 5-nitro-2-phenyl -1-ethyl benzimidazol (5), 2- (p-bromophenyl)- 5-nitro- 1-ethyl benzimidazol (6), 2- (p-bromophenyl-5-nitro-1–cyclopentyl benzimidazol (7), 2- (p-bromophenyl) -5-nitro-1-cyclopentyl benzimidazol (8), 5-amino-2-(p-bromophenyl)-1-ethylbenzimidazol (9) and 5-amino-2-(p-bromophenyl)-1-cyclopentyl benzimidazol (10) were synthesized. The structures of all the synthesized compounds were elucidated by using elemental analysis and different spectroscopic techniques (IR, NMR and mass spectroscopy). Some of these compounds showed potential antifungal

APA, Harvard, Vancouver, ISO, and other styles

6

Külen, Seda, and Sebla Dincer. "Evaluation of the effects of some benzimidazole derivatives on germination parameters of wheat varieties." Journal of Agricultural Sciences, Belgrade 69, no. 2 (2024): 121–34. http://dx.doi.org/10.2298/jas2402121k.

Full text

Abstract:

This study aims to investigate the effect of some benzimidazole derivatives on the germination parameters of bread and durum wheat varieties. These derivatives contain both unsubstituted and substituted benzimidazole structures to determine the effect of the substituents on germination. Three different durum wheat varieties (?e?it-1252, Eminbey, and K?z?ltan-91) and three different bread wheat varieties (Demir 2000, Bayraktar 2000, and Tosunbey) were used in the study. First, 1H-benzimidazole (1) and 5-nitro-1H-benzimidazole (2) compounds were used to synthesize dinitro compounds (5,6-dnitro-1

APA, Harvard, Vancouver, ISO, and other styles

7

Ma, Qing Yu, Rui Fang Guan, and Guo Zhong Li. "Two Novel Tetrahedrally Silicon-Based Benzimidazole Derivatives: Potentials as Blue Emitters for OLEDs." Advanced Materials Research 306-307 (August 2011): 206–10. http://dx.doi.org/10.4028/www.scientific.net/amr.306-307.206.

Full text

Abstract:

Two novel silicon-centered benzimidazole derivatives, Bis(4-(benzimidazol-1-yl)phenyl) dimethylsilane (1) and Bis(3-(benzimidazol-1-yl)phenyl)dimethylsilane (2) have been synthesized and determined by IR, 1H NMR, 13C NMR and mass spectroscopy. These compounds have high thermal stability and are fluorescent with emission in the region of violet to blue, which could be potentially applied as blue emitters in organic light-emitting diodes (OLEDs) display.

APA, Harvard, Vancouver, ISO, and other styles

8

Geiger, H. Cristina, Patricia L. Zick, William R. Roberts, and David K. Geiger. "Synthesis and characterization of a novel long-alkyl-chain ester-substituted benzimidazole gelator and its octan-1-ol solvate." Acta Crystallographica Section C Structural Chemistry 73, no. 4 (2017): 350–56. http://dx.doi.org/10.1107/s2053229617004314.

Full text

Abstract:

The synthesis of a novel benzimidazole derivative with a long-chain-ester substituent, namely methyl 8-[4-(1H-benzimidazol-2-yl)phenoxy]octanoate, (3), is reported. Ester (3) shows evidence of aggregation in solution and weak gelation ability with toluene. The octan-1-ol solvate, methyl 8-[4-(1H-benzimidazol-2-yl)phenoxy]octanoate octan-1-ol monosolvate, C22H26N2O3·C8H18O, (4), exhibits a four-molecule hydrogen-bonded motif in the solid state, with N—H...O hydrogen bonds between benzimidazole molecules and O—H...N hydrogen bonds between the octan-1-ol solvent molecules and the benzimidazole un

APA, Harvard, Vancouver, ISO, and other styles

9

Poddar, Saikat Kumar, Nazmus Saqueeb, and SM Abdur Rahman. "Synthesis and Biological Evaluation of 2-methyl-1Hbenzimidazole and 1H-benzimidazol-2-yl-methanol." Dhaka University Journal of Pharmaceutical Sciences 15, no. 1 (2016): 83–87. http://dx.doi.org/10.3329/dujps.v15i1.29201.

Full text

Abstract:

Two benzimidazole derivatives namely 2-methyl-1H-benzimidazole (1) and 1H-benzimidazol-2- ylmethanol (2) were synthesized in high yields by condensing O-phenylenediamine with two different carboxylic acid derivatives: glacial acetic acid and glycolic acid, following a different synthetic protocol. Structures were elucidated by spectroscopic methods. Among the two benzimidazole derivatives synthesized, 2-methyl-1Hbenzimidazole (1) showed moderate antioxidant activity with IC50 values of 144.84?g/ml whereas 1H-benzimidazol- 2-ylmethanol (2) displayed mild antioxidant activity (IC50 value 400.42

APA, Harvard, Vancouver, ISO, and other styles

10

Patel, Darshana D., and Vikram N. Panchal. "Studies on Metal Complexes of Pyrazole Bearing Ligand with Their Antimicrobial Screening." Oriental Journal Of Chemistry 40, no. 5 (2024): 1394–98. http://dx.doi.org/10.13005/ojc/400522.

Full text

Abstract:

In present research article, we reported the synthesise of novel hetertocyclic ligand namely,5-((3-((1H-benzimidazol-1-yl)methyl)-5-phenyl-1H-pyrazol-1-yl) methyl)-8-hydroxy quinoline (BIPPHQ) from 5-chloro methyl-8-hydroxy quinoline and 1-((5-phenyl-1H-pyrazol-3-yl) methyl)-1H-benzimidazole (BIPP). The BIPP was synthsised by the reaction between hydrazine hydrate with 1-(1H-benzimidazol-1-yl)-4-phenylbut-3-en-2-one (BIPB), which was synthesisd from 1-(1H-benzimidazol-1-yl)propan-2-one (BIP) and benzaldehyde. The transition metal complxes of 5-((3-((1H-benzimidazol-1-yl)methyl)-5-phenyl-1H-pyr

APA, Harvard, Vancouver, ISO, and other styles

11

Martin, RF, M. Pardee, DP Kelly, and POL Mack. "Synthesis and Characterization of 2-Iodo-4-[5′-(4'″-Methylpiperazin-1'″-yl)-2′,5′-bi-1h-Benzimidazol-2 ′-Yl]Phenol (iodoHoechst 33258) and 2,5-Disubstituted Benzimidazole Model Compounds." Australian Journal of Chemistry 39, no. 2 (1986): 373. http://dx.doi.org/10.1071/ch9860373.

Full text

Abstract:

The product of iodination of the DNA-binding dye Hoechst 33258,4-[5′- (4′′′-methylpiperazin-1′′′-yl)-2′,5′-bi-1H-benzimidazol-2′-yl]phenol (1), has been identified as the monoiodo derivative, i.e. 2-iodo-4-[5′- (4′′′-methylpiperazin-1′′′-yl)-2′,5′-bi-1H-benzimidazol-2′-yl]phenol (2), by mass spectrometry and by comparison of the 1H and 13C n.m.r . spectra of (1) and (2) with those of 2,5-disubstituted benzimidazole model compounds (3) and (4).

APA, Harvard, Vancouver, ISO, and other styles

12

Goossens, Laurence, Omar Castillo-Aguilera, Patrick Depreux, Alexia Ballée, Florian Beaurain, and Paola B. Arimondo. "Study of the Effect of Substituents of ortho-Phenylenediamines in the Opening of Lactones and Lactams for Access to Benzimidazol-2-yl Alkanols and Benzimidazol-2-yl Alkylamines." Synlett 31, no. 12 (2020): 1216–20. http://dx.doi.org/10.1055/s-0040-1707112.

Full text

Abstract:

Benzimidazoles represent common chemical moieties in bioactive compounds. The synthesis of this heterocycle often involves a condensation of an ortho-phenylenediamine with a carboxylic acid derivative. The observed dialkylation of the starting ortho-phenylenediamine is avoided by opening of lactones or lactams. This strategy can directly yield 1H-benzimidazoles substituted at the 2-position by a functionalized chain. We present herein a study of the effect of different electron-withdrawing or electron-donating groups at the 4-position of ortho-phenylenediamines on the opening of lactones or la

APA, Harvard, Vancouver, ISO, and other styles

13

Potikha, Lyudmyla M., Volodymyr V. Sypchenko, and Valentyn I. Davydov. "Reactions of [2-(Bromomethyl)phenyl](4-chlorophenyl)methanone: A New Synthesis of [1,3]Thiazolo[3,2-b][2,4]benzodiazepine, Benzimidazo[1,2-b][2,4]benzodiazepine and Benzimidazo[1,2-b][2]benzazepine Derivatives." French-Ukrainian Journal of Chemistry 7, no. 1 (2019): 96–103. http://dx.doi.org/10.17721/fujcv7i1p96-103.

Full text

Abstract:

A new approach to the development of a number of azolo-condensed azepines and diazepines has been proposed. The method for the synthesis of [1,3]thiazolo[3,2-b][2,4]benzodiazepine, benzimidazo[1,2-b][2,4]benzodiazepineandbenzimidazo[1,2-b][2]benzazepinederivatives involves the reaction of [2-(bromomethyl)phenyl](4-chlorophenyl)methanonewith5-methyl-1,3-thiazol-2-amine, 1H-benzimidazol-2-amineand1,2-dimethyl-1H-benzimidazole. The formation of the quaternary salt of the initial diazole has been done under mild conditions in MeCN. The following intramolecular condensation has been realized by hea

APA, Harvard, Vancouver, ISO, and other styles

14

Zaderenko, P., M. S. Gil, P. López, P. Ballesteros, I. Fonseca, and A. Albert. "Diethyl 2-Benzimidazol-1-ylsuccinate–Picric Acid (1/1) – An Inclusion Molecular Complex." Acta Crystallographica Section B Structural Science 53, no. 6 (1997): 961–67. http://dx.doi.org/10.1107/s0108768197008562.

Full text

Abstract:

The crystal structure of the diethyl 2-benzimidazol-1-ylsuccinate–picric acid (1/1) molecular complex has been determined by X-ray diffraction analysis. Diethyl 2-benzimidazol-l-ylsuccinate molecules form channels along the a axis, in which the picric acid molecules are located. The benzimidazole moiety and the phenol group are held together by hydrogen bonding between the hydrogen of the phenol and the N3 atom of benzimidazole. Additionally, this hydrogen forms an intramolecular hydrogen bond with one O atom of the ortho-nitro group, thus producing a bifurcated hydrogen bond. 1H NMR spectra i

APA, Harvard, Vancouver, ISO, and other styles

15

Kayukova, L. A., A. V. Vologzhanina, A. Yerlanuly та A. M. Duisenali. "THE BASE PRESENCE AT THE ALKYLSULFOCHLORINATION OF β-AMINOPROPIOAMIDOXIMES IN CHLOROFORM AND WATER". Chemical Journal of Kazakhstan 86, № 2 (2024): 36–41. http://dx.doi.org/10.51580/2024-2.2710-1185.19.

Full text

Abstract:

We have studied the regioselectivity of alkylsulfochlorination of β-(4-phenylpiperazin-1-yl)- and β-(benzimidazol-1-yl)-propioamidoximes using AlkSO2Cl under two conditions: (i) in chloroform in the presence of tributylamine (Bu3N) as a base at room temperature (r.t.); (ii) in water and acetone (4:1) without Bu3N at r.t. The reaction under the conditions (i) leads to the return of the original amidoximes, the formation of 2-amino-8-phenyl-1,5,8-triazaspiro[4.5]dec-1-ene-5-ammonium chloride and β-(benzimidazole-1-yl)propioamidoxime hydrochloride. When alkylsulfochlorination occurs under conditi

APA, Harvard, Vancouver, ISO, and other styles

16

Zhang, Yue-Feng, Jian-Ping Ma, Qi-Kui Liu, and Yu-Bin Dong. "Three isomorphous two-dimensional coordination polymers generated from a benzimidazole bridging ligand and ZnX2(X= Cl, Br and I)." Acta Crystallographica Section C Crystal Structure Communications 69, no. 4 (2013): 367–71. http://dx.doi.org/10.1107/s0108270113005982.

Full text

Abstract:

A novel bridging asymmetric benzimidazole ligand, 4-{2-[3-(pyridin-4-yl)phenyl]-1H-benzimidazol-1-ylmethyl}benzoic acid, was used to construct three isomorphous two-dimensional coordination polymers, namelycatena-poly[chlorido(μ3-4-{2-[3-(pyridin-4-yl)phenyl]-1H-benzimidazol-1-ylmethyl}benzoato)zinc(II)], [Zn(C26H18N3O2)Cl]n, (I), and the bromide, (II), and iodide, (III), analogues. Neighbouring two-dimensional networks are stacked into three-dimensional frameworksviainterlayer π–π interactions. The luminescent properties of (I)–(III) were investigated and they display an obvious red-shift in

APA, Harvard, Vancouver, ISO, and other styles

17

Sarnit, E., V. Cikalov, A. Poddubov, and D. Peroshkova. "SYNTHESIS AND PREDICTED ANTI-TUBERCULOSIS ACTIVITY OF DERIVATIVES OF (2-METHYL-1H-BENZIMIDAZOLE-1-YL)ETHANOIC AND (5,6-DIMETHYL-1H-BENZIMIDAZOLE-1-YL)ETHANOIC ACIDS." Scientific Notes of V.I. Vernadsky Crimean Federal University. Biology. Chemistry 11, no. 1 (2025): 310–20. https://doi.org/10.29039/2413-1725-2025-11-1-310-320.

Full text

Abstract:

In this work, hydrazides, salicylidenehydrazones and 1,2,4-triazoles (2-methyl-1H-benzimidazol-1-yl)ethanoic and (5,6-dimethyl-1H-benzimidazol-1-yl)ethanoic acids were synthesized and studied. It was shown that standard methods for the synthesis of hydrazides, acylhydrazones and triazoles are also applicable to benzimidazole derivatives. The conversion of hydrazides to salicylidene hydrazones and 1,2,4-triazoles leads to an increase in the stability of the compounds, since. Storing hydrazides of these acids in air leads to their slow oxidation. A prediction was made of the potential biological

APA, Harvard, Vancouver, ISO, and other styles

18

Mamedov, Vakhid A. "Recent advances in the synthesis of benzimidazol(on)es via rearrangements of quinoxalin(on)es." RSC Advances 6, no. 48 (2016): 42132–72. http://dx.doi.org/10.1039/c6ra03907c.

Full text

Abstract:

The review describes all the quinoxaline-benzimidazole rearrangements as a whole and the new quinoxalinone-benzimidazol(on)e rearrangements in particular when exposed to nucleophilic rearrangements which can be used for the synthesis of various biheterocyclic motifs.

APA, Harvard, Vancouver, ISO, and other styles

19

Ansari, K. F., C. Lal, and R. K. Khitoliya. "Synthesis and biological activity of some triazole-bearing benzimidazole derivatives." Journal of the Serbian Chemical Society 76, no. 3 (2011): 341–52. http://dx.doi.org/10.2298/jsc100301029a.

Full text

Abstract:

A number of N'-[(aryl)methylidene]-2-(2-methyl-1H-benzimidazol- 1-yl)acetohydrazide and 4-(aryl)-5-[(2-methyl-1H-benzimidazol- 1-yl)methyl]-4H-1,2,4-triazole-3-thiol derivatives were synthesized by incorporating various aromatic and heterocyclic substituents on 2-methyl-1H-benzimidazole. The structures of all the synthesized compounds were elucidated based on their elemental analyses and spectral data. The in vitro activities of these compounds against bacteria and fungi were evaluated by the disc diffusion and the minimum inhibitory concentration (MIC) methods. Some of the synthesized derivat

APA, Harvard, Vancouver, ISO, and other styles

20

Ubeid, Mustafa Turki, Hamdy Khamees Thabet, and Mohamed Yousef Abu Shuheil. "Synthesis of 4-[(1H-Benzimidazol-2-yl)sulfanyl]benzaldehyde and 2-({4-[(1H-Benzimidazol-2-yl)sulfanyl]phenyl}methylidene)hydrazine-1-carbothioamide." Molbank 2021, no. 3 (2021): M1273. http://dx.doi.org/10.3390/m1273.

Full text

Abstract:

Here we describe the preparation of 2-(4-((1H-benzo[d]imidazol-2-yl)thio)-benzylidene)-hydrazine-1-carbothioamide in two steps. In the first step, 1,3-dihydro-2H-1,3-benzimidazole-2-thione was reacted with 4-fluorobenzaldehyde in DMSO to get 4-[(1H-benzimidazol-2-yl)sulfanyl]benzaldehyde in high yield. The reaction of the obtained aldehyde with thiosemicarbazide in ethanol at reflux temperature yielded 2-({4-[(1H-benzimidazol-2-yl)sulfanyl]phenyl}methylidene)hydrazine-1-carbothioamide. The structure of the synthesized compounds was established by NMR spectroscopy (1H, 13C), mass spectrometry,

APA, Harvard, Vancouver, ISO, and other styles

21

Rathore, Kavita, Usha Ameta, Swati Ojha, Ranjana Sharma, and G. L. Talesara. "Synthesis and Antibiotic Activity of Mebendazole Derivatives of Pharmacological Interest." E-Journal of Chemistry 4, no. 2 (2007): 166–72. http://dx.doi.org/10.1155/2007/503952.

Full text

Abstract:

Mebendazole is a well known anti-helimintic and belongs to the benzimidazole group of medicines. In order to achieve better medicinal results, i.e. enhanced activity and low toxicity, structural modifications are made in the existing drugs. Some 5-benzoyl-N-[1-(alkoxyphthalimido) benzimidazol-2-yl] carbamic acid methyl ester(3a-c)and 5-benzoyl-N-[1-(2,3-bis oxyphthalimido∕oxysuccinimido propyl benzimidazol-2-yl) carbamic acid methyl ester(7a-b)have been synthesized from two different routes. Structures of the compounds have been established on the basis of elemental analysis and spectral studi

APA, Harvard, Vancouver, ISO, and other styles

22

Li, Yan-an, Qi-Kui Liu, Jian-Ping Ma, and Yu-Bin Dong. "3,5-Bis{4-[(benzimidazol-1-yl)methyl]phenyl}-4H-1,2,4-triazol-4-amine and its one-dimensional polymeric complex with HgCl2." Acta Crystallographica Section C Crystal Structure Communications 68, no. 6 (2012): m152—m155. http://dx.doi.org/10.1107/s0108270112019233.

Full text

Abstract:

The molecule of 3,5-bis{4-[(benzimidazol-1-yl)methyl]phenyl}-4H-1,2,4-triazol-4-amine (L), C30H24N8, has an antiperiplanar conformation of the two terminal benzimidazole groups and forms two-dimensional networks along the crystallographicbaxisviatwo types of intermolecular hydrogen bonds. However, incatena-poly[[[dichloridomercury(II)]-μ-3,5-bis{4-[(benzimidazol-1-yl)methyl]phenyl}-4H-1,2,4-triazol-4-amine] dichloromethane hemisolvate], {[HgCl2(C30H24N8)]·0.5CH2Cl2}n, synthesized by the combination ofLwith HgCl2, theLligand adopts a synperiplanar conformation. The HgIIcation lies in a distorte

APA, Harvard, Vancouver, ISO, and other styles

23

Singh, Raj P., and Mikio Chiba. "Reversed-Phase Liquid Chromatographic Method for the Simultaneous Determination of Benomyl and Methyl lH-Benzimidazol-2-ylcarbamate in Wettable Powder Formulations." Journal of AOAC INTERNATIONAL 76, no. 6 (1993): 1187–92. http://dx.doi.org/10.1093/jaoac/76.6.1187.

Full text

Abstract:

Abstract A liquid chromatographic (LC) method is reported for the simultaneous determination of benomyl, methyl {1 -[(butylamino)carbonyl]-1 H-benzimidazol-2-yl}carbamate and carbendazim, methyl 1H-benzimidazol-2-ylcarbamate (MBC), in wettable powder (WP) formulations. In this method, benomyl is converted to 3-butyl-2,4-dioxo-s-triaz-ino[1,2-a]benzimidazole (STB) in 0.125M sodium hydroxide. After conversion (at room temperature in 20 min), STB is determined simultaneously with MBC (which remains intact with the sodium hydroxide treatment) at 286 nm after LC separation on a C18 column. The meth

APA, Harvard, Vancouver, ISO, and other styles

24

Ashrafi, Amir M., Pavel Kopel, and Lukas Richtera. "An Investigation on the Electrochemical Behavior and Antibacterial and Cytotoxic Activity of Nickel Trithiocyanurate Complexes." Materials 13, no. 7 (2020): 1782. http://dx.doi.org/10.3390/ma13071782.

Full text

Abstract:

The electrochemical redox behavior of three trinuclear Ni(II) complexes [Ni3(abb)3(H2O)3(µ-ttc)](ClO4)3 (1), [Ni3(tebb)3(H2O)3(µ-ttc)](ClO4)3·H2O (2), and [Ni3(pmdien)3(µ-ttc)](ClO4)3 (3), where abb = 1-(1H-benzimidazol-2-yl)-N-(1H-benzimidazol-2-ylmethyl)methan-amine, ttcH3 = trithiocyanuric acid, tebb = 2-[2-[2-(1H-benzimidazol-2-yl)ethylsulfanyl]ethyl]-1H-benzimidazole, and pmdien = N,N,N′,N″,N″-pentamethyldiethylenetriamine is reported. Cyclic voltammetry (CV) was applied for the study of the electrochemical behavior of these compounds. The results confirmed the presence of ttc and nickel

APA, Harvard, Vancouver, ISO, and other styles

25

Indusegaram, Sutharsiny, Andrew G. Katsifis, Damon D. Ridley, and Simone C. Vonwiller. "Nitrogen versus Oxygen Group Protection in Hydroxypropylbenzimidazoles." Australian Journal of Chemistry 56, no. 8 (2003): 819. http://dx.doi.org/10.1071/ch03012.

Full text

Abstract:

In order to convert 1′H-benzimidazol-2′-ylpropanols into aryl ethers using Mitsunobu coupling, it was necessary to protect the benzimidazole nitrogen in the starting alcohols. Selective protection at nitrogen was achieved through N-benzyl derivatives, but attempts to protect the nitrogen directly through tert-butoxycarbonyl, acetyl, trityl, or tetrahydropyranyl derivatives were complicated either by selective reactions at oxygen or by the formation of bis-protected compounds. Transformations of some oxygen-protected derivatives are discussed, and in particular the conversion of the acetates of

APA, Harvard, Vancouver, ISO, and other styles

26

Hu, Dong-Cheng, Chao-Hu Xiao, Guo-Zhe Guo, Yun-Xia Yang, and Jia-Cheng Liu. "A one-dimensional silver(I) coordination polymer based on the 2-[2-(pyridin-4-yl)-1H-benzimidazol-1-ylmethyl]phenol ligand exhibiting photoluminescence." Acta Crystallographica Section C Crystal Structure Communications 69, no. 4 (2013): 356–59. http://dx.doi.org/10.1107/s0108270113005817.

Full text

Abstract:

A one-dimensional AgIcoordination complex,catena-poly[[silver(I)-μ-{2-[2-(pyridin-4-yl)-1H-benzimidazol-1-ylmethyl]phenol-κ2N2:N3}] perchlorate monohydrate], {[Ag(C19H15N3O)]ClO4·H2O}n, was synthesized by the reaction of 2-[2-(pyridin-4-yl)-1H-benzimidazol-1-ylmethyl]phenol (L) with silver perchlorate. In the complex, theLligands are arranged alternately and link AgIcations through one benzimidazole N atom and the N atom of the pyridine ring, leading to an extended zigzag chain structure. In addition, the one-dimensional chains are extended into a three-dimensional supramolecular architecturev

APA, Harvard, Vancouver, ISO, and other styles

27

Temel, Halide Edip, Gülşen Akalın Çiftçi, and Leyla Yurttaş. "Screening of new morpholine dithiocarbamate derivatives bearing benzimidazole moiety for anticholinesterase potential." European Journal of Life Sciences 2, no. 2 (2023): 71–77. http://dx.doi.org/10.55971/ejls.1328405.

Full text

Abstract:

Alzheimer’s disease (AD) is basically associated with disturbances of cholinesterase metabolism which result in acetylcholine deficiency. Target of acetylcholinesterase (AChE) inhibitors used in symptomatic therapy of disease is to increase of ACh levels. Consequently, cholinesterase inhibitors were developed to increase acetylcholine is to inhibit AChE and butrylcholinesterase (BuChE). Studies demonstrate the clinical importance of dual inhibitors that inhibit not only the acetylcholinesterase enzyme but also the butyrylcholinesterase enzyme. In recent years, benzimidazoles have attracted par

APA, Harvard, Vancouver, ISO, and other styles

28

Conboy, Darren, and Fawaz Aldabbagh. "6-Imino-1,2,3,4,8,9,10,11-octahydropyrido[1,2-a]pyrido[1′,2′:1,2]imidazo[4,5-f]benzimidazole-13-one: Synthesis and Cytotoxicity Evaluation." Molbank 2020, no. 1 (2020): M1118. http://dx.doi.org/10.3390/m1118.

Full text

Abstract:

The first report of an iminoquinone of imidazo[4,5-f]benzimidazole is described. The 2D-NOESY spectrum of 1,2,3,4,8,9,10,11-octahydropyrido[1,2-a]pyrido[1’,2’:1,2]imidazo[4,5-f]benzimidazol-6-amine was used to confirm the location of the imine moiety at the C-6 position of the title compound. Cytotoxicity data from the National Cancer Institute are included.

APA, Harvard, Vancouver, ISO, and other styles

29

Patricio-Rangel, Emmanuel Blas, Margarita Tlahuextl, Hugo Tlahuext, and Antonio Rafael Tapia-Benavides. "Synthesis and crystallographic studies of two new 1,3,5-triazines." Acta Crystallographica Section C Structural Chemistry 76, no. 4 (2020): 322–27. http://dx.doi.org/10.1107/s2053229620002508.

Full text

Abstract:

The synthesis and characterization of two new 1,3,5-triazines containing 2-(aminomethyl)-1H-benzimidazole hydrochloride as a substituent are reported, namely, 2-{[(4,6-dichloro-1,3,5-triazin-2-yl)amino]methyl}-1H-benzimidazol-3-ium chloride, C11H9Cl2N6 +·Cl− (1), and bis(2,2′-{[(6-chloro-1,3,5-triazine-2,4-diyl)bis(azanediyl)]bis(methylene)}bis(1H-benzimidazol-3-ium)) tetrachloride heptahydrate, 2C19H18ClN9 2+·4Cl−·7H2O (2). Both salts were characterized using single-crystal X-ray diffraction analysis and IR spectroscopy. Moreover, the NMR (1H and 13C) spectra of 1 were obtained. Salts 1 and 2

APA, Harvard, Vancouver, ISO, and other styles

30

Kouassi Yves Guillaume MOLOU, Tchambaga Etienne CAMARA, Adeyolé TIMOTOU, et al. "Design, synthesis of bisbenzimidazole dithiol derivatives and analogs." GSC Advanced Research and Reviews 13, no. 2 (2022): 085–90. http://dx.doi.org/10.30574/gscarr.2022.13.2.0300.

Full text

Abstract:

The benzimidazole scaffold is an important pharmacophore and one of the preferred structures in medicinal chemistry due to the wide range of biological activities of its derivatives. Here in this article, the synthesis of two series of compounds, namely bis(thiobenzimidazol-2-yl)methane derivatives and analogs (4a-e) and bis(benzimidazol-2-yl)dithiol derivatives and analogs (5a-e) are described. These compounds were synthesized by first designing 2-mercaptobenzimidazole derivatives and analogs (2a-e) by action of orthophenylenediamine and analogs (1a-e) with carbon disulfide. Reaction of thiol

APA, Harvard, Vancouver, ISO, and other styles

31

Kouassi, Yves Guillaume MOLOU, Etienne CAMARA Tchambaga, TIMOTOU Adeyolé, et al. "Design, synthesis of bisbenzimidazole dithiol derivatives and analogs." GSC Advanced Research and Reviews 13, no. 2 (2022): 085–90. https://doi.org/10.5281/zenodo.7668593.

Full text

Abstract:

The benzimidazole scaffold is an important pharmacophore and one of the preferred structures in medicinal chemistry due to the wide range of biological activities of its derivatives. Here in this article, the synthesis of two series of compounds, namely bis(thiobenzimidazol-2-yl)methane derivatives and analogs (4a-e) and bis(benzimidazol-2-yl)dithiol derivatives and analogs (5a-e) are described. These compounds were synthesized by first designing 2-mercaptobenzimidazole derivatives and analogs (2a-e) by action of orthophenylenediamine and analogs (1a-e) with carbon disulfide. Reaction of thiol

APA, Harvard, Vancouver, ISO, and other styles

32

Hsieh, Ko, Chang, et al. "Design and Synthesis of Benzimidazole-Chalcone Derivatives as Potential Anticancer Agents." Molecules 24, no. 18 (2019): 3259. http://dx.doi.org/10.3390/molecules24183259.

Full text

Abstract:

Numerous reports have shown that conjugated benzimidazole derivatives possess various kinds of biological activities, including anticancer properties. In this report, we designed and synthesized 24 new molecules comprising a benzimidazole ring, arene, and alkyl chain-bearing cyclic moieties. The results showed that the N-substituted benzimidazole derivatives bearing an alkyl chain and a nitrogen-containing 5- or 6-membered ring enhanced the cytotoxic effects on human breast adenocarcinoma (MCF-7) and human ovarian carcinoma (OVCAR-3) cell lines. Among the 24 synthesized compounds, (2E)-1-(1-(3

APA, Harvard, Vancouver, ISO, and other styles

33

Bai, Song, Miaohe Zhang, Shouying Tang, et al. "Research Progress on Benzimidazole Fungicides: A Review." Molecules 29, no. 6 (2024): 1218. http://dx.doi.org/10.3390/molecules29061218.

Full text

Abstract:

Benzimidazole fungicides are a class of highly effective, low-toxicity, systemic broad-spectrum fungicides developed in the 1960s and 1970s, based on the fungicidal activity of the benzimidazole ring structure. They exhibit biological activities including anticancer, antibacterial, and antiparasitic effects. Due to their particularly outstanding antibacterial properties, they are widely used in agriculture to prevent and control various plant diseases caused by fungi. The main products of benzimidazole fungicides include benomyl, carbendazim, thiabendazole, albendazole, thiophanate, thiophanat

APA, Harvard, Vancouver, ISO, and other styles

34

Cole, ER, G. Crank, and i. Sumantr. "Oxidations With Lead-Tetraacetate. VI. Oxidations of Benzimidazoles, Benzoxazoles and Benzothiazoles." Australian Journal of Chemistry 39, no. 2 (1986): 295. http://dx.doi.org/10.1071/ch9860295.

Full text

Abstract:

Benzimidazole is slowly oxidized in the imidazole ring by lead tetraacetate to benzimidazol-2(3H)-one, 1-acetylbenzimidazol-2(3H)-one and N,N′-(o- phenylene ) bisacetamide . With excess oxidant, oxidation also occurs in the benzene ring at C5. Benzoxazole is much more reactive and gives a variety of products formed by oxidation of both rings. Benzothiazole is the least reactive system and suffers only minimal oxidation at C2 of the thiazole ring.

APA, Harvard, Vancouver, ISO, and other styles

35

Belousova, Z. P., N. A. Klenova, and I. A. Makeeva. "EFFECT OF PHENOLIC DERIVATIVES OF BENZIMIDAZOLE ON GROWTH AND ENZYME ACTIVITY OF E. COLI." Vestnik of Samara University. Natural Science Series 19, no. 9.1 (2017): 122–27. http://dx.doi.org/10.18287/2541-7525-2013-19-9.1-122-127.

Full text

Abstract:

Dose-response stady (concentration of 50-200 mkg/ml) effect on growth total degidrogenase, catalase, sukcinatdegidrogenase activity of E. COLI phenolic benzimidazole derivatives containing a methyl group and the glycoside radical is researched. All compounds have dozo-respouse bacteriostatic effect and cause metabolic stress, resulting in higher concentrations of active degidrogenase and catalase. Most damaging effect has 4(2-methyl-1fi-benzimidazol-ylmethyl)phenyl-2,3,4,6-tetra-O-azethyl-/3-D-glucopyranozyd in a concentration of 200 mkg/ml.

APA, Harvard, Vancouver, ISO, and other styles

36

Kordian, Marcus, Holger Feist, and Klaus Peseke. "Anellation and Ring Transformations of Push-pull-functionalized Deoxypyranosiduloses." Zeitschrift für Naturforschung B 64, no. 6 (2009): 676–82. http://dx.doi.org/10.1515/znb-2009-0613.

Full text

Abstract:

Reaction of (E)-3-aminomethylene-α-D-erythro-hexopyranosid-2-ulose 5 with substituted 5- aminopyrazoles afforded the pyrano-anellated pyrazolo[1,5-a]pyrimidines 8. The treatment of the corresponding (E)-2-aminomethylene-α-D-erythro-hexopyranosid-3-ulose 6 with 5-aminopyrazoles and (benzimidazol-2-yl)acetonitrile yielded in a ring transformation process the D-erythronoyl-pyrazolo[ 1,5-a]pyrimidine-3-carbonic acid derivatives 10 and D-erythronoyl-pyrido[1,2-a]benzimidazole- 4-carbonitrile (12), respectively

APA, Harvard, Vancouver, ISO, and other styles

37

Kheder, Nabila A., Yahia N. Mabkhot, Fawzia R. Zahian, and Sara S. Mohamed. "Regioselective Synthesis of Some Pyrazole Scaffolds Attached to Benzothiazole and Benzimidazole Moieties." Journal of Chemistry 2014 (2014): 1–5. http://dx.doi.org/10.1155/2014/581721.

Full text

Abstract:

Condensation of 2-(benzothiazol-2-yl)acetonitrile (1) or 2-(1-methyl-1H-benzimidazol-2-yl)acetonitrile (2) with thiophene-2-carbaldehyde afforded the corresponding acrylonitrile derivatives3or4, respectively. The 1,3-dipolar cycloaddition reaction of the acrylonitrile3or4with nitrile-imine6gave novel pyrazole derivatives pendant to benzothiazole and benzimidazole. The pyrazoline derivative7was converted into the corresponding pyrazole derivative11via thermal elimination of hydrogen cyanide upon heating in sodium ethoxide solution. The structures of the synthesized products were confirmed by IR

APA, Harvard, Vancouver, ISO, and other styles

38

Abe, Noritaka, Hiroyuki Fujii, Akikazu Kakehi, and Motoo Shiro. "Revised Structures, 1-Methylene-1H-[1,4]thiazino[4,3-a]-benzimidazole and 10-Methylene-10H-imidazo[2,1-c][1,4]-benzothiazine Derivatives, for the Cycloadducts Accompanying Rearrangement from Imidazo[2,1-b]benzothiazole and Thiazolo [3,2-a] benzimidazole Derivatives with Propiolic Esters." Journal of Chemical Research 23, no. 5 (1999): 322–23. http://dx.doi.org/10.1177/174751989902300513.

Full text

Abstract:

Formerly-proposed structures, thiazolo[3,2- a] [1,5]benzodiazepine and [1,4]diazepino[7,1- b]benzothiazole derivatives, cycloadducts from the reactions of thiazolo[3,2- a] benzimidazole and imidazo[2,1- b]benzothiazole derivatives with propiolic esters, are revised to methyl 2-[4-methyl-( E)-1 H-[1,4]thiazino[4,3- a]benzimidazol-1-ylidene)methoxycarbonylmethyl]-( E)-acrylate and methyl [2-methyl-( E)-10 H-imidazo[2,1- c] [1,4]benzothiazine-10-ylidene)-methoxycarbonylmethyl]-( E)-acrylate, respectively, whose structures are deduced by X-ray structure analysis.

APA, Harvard, Vancouver, ISO, and other styles

39

Rakhmonova, Dilnoza, Zukhra Kadirova, Batirbay Torambetov, Shakhnoza Kadirova, Jamshid Ashurov, and Svitlana Shishkina. "The molecular and crystal structures of 2-(3-hydroxypropyl)benzimidazole and its nitrate salt." Acta Crystallographica Section E Crystallographic Communications 78, no. 2 (2022): 211–15. http://dx.doi.org/10.1107/s2056989022000585.

Full text

Abstract:

2-(3-Hydroxypropyl)-1H-benzimidazole, C10H12N2O, which has potential biological activity, can be used as a ligand for complexation with metals. This compound is an electron donor, due to the lone pair of the nitrogen atom in the imidazole ring. This nitrogen atom also acts as a proton acceptor. In the crystalline phase, the nitrate salt, namely, 2-(3-hydroxypropyl)-1H-benzimidazol-3-ium nitrate, C10H13N2O+·NO3 −, has been studied. The protonation of the 2-(3-hydroxypropyl)benzimidazole unit results in significant delocalization of the electron density within the imidazole ring. The salt format

APA, Harvard, Vancouver, ISO, and other styles

40

Khamidova, T. V., E. V. Kozhevnikova, V. G. Kiryukhin, and B. N. Filatov. "On the problem of secondary prevention of hepatotropic manifestations of dioxyne intoxication." Kazan medical journal 78, no. 1 (1997): 55–57. http://dx.doi.org/10.17816/kazmj81123.

Full text

Abstract:

The liver morphology in intoxication by 2-(a-fluor-a-trifhiormethoxymethyl) benzimidazol, 2-a- hydrotetrafluorethy) benzimidazol and 5 (6)-(2-oxy-hexafluorisopropil)-2-(a-fluor-a-trifluormethoxymethyl) benzimidazol is studied experimentally on rats. Vaseline oil in large doses manifests hepatoprotector property early in intoxication.

APA, Harvard, Vancouver, ISO, and other styles

41

Tomović, Katarina, Jelena Mrmošanin, Denitsa Yancheva, Anelia Mavrova, and Andrija Šmelcerović. "In vitro antioxidant properties of 2-imino-benzimidazole and 1,3-thiazolo[3,2-a]benzimidazolone derivatives." Acta Facultatis Medicae Naissensis 37, no. 4 (2020): 381–86. http://dx.doi.org/10.5937/afmnai37-27103.

Full text

Abstract:

Antioxidant properties of 2-[2-imino-5-nitro-3-(2-oxo-2-phenylethyl)-2,3-dihydro-1H-benzimidazol1-yl]-1-phenylethanone (compound 1) and 2-(4-fluorobenzylidene)-6-(phenylcarbonyl)[1,3]thiazolo[3,2a]benzimidazol-3(2H)-one (compound 2) were evaluated in vitro. Compounds 1 and 2 did not show significant radical scavenging activity. It has been suggested that antioxidant strategies should not be based on direct scavengers but rather on the potentiation of endogenous antioxidant defenses, or on the reduction of the sources of reactive species. Although a direct scavenging mechanism is missing, the a

APA, Harvard, Vancouver, ISO, and other styles

42

Hafedh, Fadhel R., Hamid H. Mohammed, and Zainab N. Mageed. "Synthesis and Characterization of Novel Pyrimido [1,2-a] benzimidazole and its Derivatives." Al-Mustansiriyah Journal of Science 33, no. 1 (2022): 15–20. http://dx.doi.org/10.23851/mjs.v33i1.1020.

Full text

Abstract:

A few pyrimido[1,2-a] benzimidazole derivatives had been synthesized, derived from 4-amino-2-(4-chloro or bromophenyl) -1,2-dihydropyrimido[1,2-a] benzimidazole-3-carbonitrile (4 or 5) is made through one pot three components condensation reaction of 1H-benzimidazol-2-amine (1) with p-chloro or bromobenzaldehyde (2) and malononitrile (3). First part of these derivatives prepared by reaction compound (4 or 5) with acetic acid or propionic acid in presence POCl3 to give pyrmidino rings (6-9). Second part of derivatives were prepared by reaction compound (4 or 5) with benzoyl chloride or phenylis

APA, Harvard, Vancouver, ISO, and other styles

43

Geiger, David K., H. Cristina Geiger та Jared M. Deck. "Structure determination of three furan-substituted benzimidazoles and calculation of π–π and C—H...π interaction energies". Acta Crystallographica Section C Structural Chemistry 70, № 12 (2014): 1125–32. http://dx.doi.org/10.1107/s205322961402405x.

Full text

Abstract:

The synthesis and structural characterization of 2-(furan-2-yl)-1-(furan-2-ylmethyl)-1H-benzimidazole [C16H12N2O2, (I)], 2-(furan-2-yl)-1-(furan-2-ylmethyl)-1H-benzimidazol-3-ium chloride monohydrate [C16H13N2O2+·Cl−·H2O, (II)] and the hydrobromide salt 5,6-dimethyl-2-(furan-2-yl)-1-(furan-2-ylmethyl)-1H-benzimidazol-3-ium bromide [C18H17N2O2+·Br−, (III)] are described. Benzimidazole (I) displays two sets of aromatic interactions, each of which involves pairs of molecules in a head-to-tail arrangement. The first, denoted set (Ia), exhibits both intermolecular C—H...π interactions between the 2

APA, Harvard, Vancouver, ISO, and other styles

44

Lewis, Robert, and Alan Brook. "An Evaluation of Arbotect and Lignasan Trunk Injections as Potential Treatments for Oak Wilt in Live Oaks." Arboriculture & Urban Forestry 11, no. 4 (1985): 125–28. http://dx.doi.org/10.48044/jauf.1985.028.

Full text

Abstract:

Arbotect-20S® (2-(2)thiazolyl) benzimidazole) and Lignasan® (methyl-2-benzimidazol carbamate phosphate) were mixed with low volumes of water and injected into the xylem of live oaks in an effort to stop or prevent oak wilt (caused by Ceratocystis fagacearum) development. Healthy trees near the advancing edge of oak wilt infection centers were not protected by fungicide treatments. Some of the infected trees showed an initial slowdown in the rate of tree degeneration after injections, but after 1 5 months there was no significant difference in treated and untreated trees.

APA, Harvard, Vancouver, ISO, and other styles

45

Politano, Fabrizio, Ana K. Gran-Magano, and Nicholas E. Leadbeater. "2,2′-(1,4-Phenylene)bis(7-nitro-1H-benzimidazole 3-oxide)." Molbank 2021, no. 4 (2021): M1297. http://dx.doi.org/10.3390/m1297.

Full text

Abstract:

Bis(benzimidazol-2-yl-3-oxide)benzene derivatives have potential applications as energetic or photoactive materials. By using a two-step one-pot approach employing microwave heating as a tool, 2,2′-(1,4-phenylene)bis(7-nitro-1H-benzimidazole 3-oxide) (1) has been prepared in 94% yield. In the first step an SNAr reaction is performed using p-xylylenediamine as the central building block. Without isolating the intermediate, a base-mediated cyclization reaction follows in the second step. The product was isolated in analytically pure form by means of a pH-controlled precipitation.

APA, Harvard, Vancouver, ISO, and other styles

46

Engin, Saka, Akkoç Senem, and Coban Burak. "Synthesis, DNA Interaction and Cytotoxic Activity Studies of a Novel 2,1,3-Benzothiadiazole-Benzimidazole Derivative." Pharmaceutical and Chemical Journal 7, no. 3 (2020): 82–89. https://doi.org/10.5281/zenodo.13954528.

Full text

Abstract:

Benzimidazoles and benzothiodiazoles are biologically active heterocyclic compounds. In here, a new compound 4-(1<em>H</em>-benzimidazol-2-yl)-7-bromo-2,1,3-benzothiodiazole containing both heterocyclic ring systems was prepared. The highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of the new compound was calculated using the Spartan 10 program. The compound binds to DNA with a moderate strength, and the cytotoxic activity studies show that the relative compound has no antiproliferative activity against cancer cell lines.

APA, Harvard, Vancouver, ISO, and other styles

47

Rani, Varsha, Harkesh B. Singh, and Ray J. Butcher. "Synthesis and structure of an arylselenenium(II) cation, [C34H41N4Se+]2[Hg(SeCN)4]2−, based on a 5-tert-butyl-1,3-bis(1-pentyl-1H-benzimidazol-2-yl)benzene scaffold." Acta Crystallographica Section E Crystallographic Communications 74, no. 6 (2018): 786–90. http://dx.doi.org/10.1107/s2056989018006394.

Full text

Abstract:

In the title salt, bis{[5-tert-butyl-1,3-bis(1-pentyl-1H-benzimidazol-2-yl)benzene]selenium} tetrakis(selenocyanato)mercury, (C34H41N4Se)2[Hg(SeCN)4], the arylselenenium cations, [C34H41N4Se]+, are linked through [Hg(SeCN)4]2−anions by C—H...N hydrogen bonds. In the cation, the geometry around the Se atom in the 5-tert-butyl-1,3-bis(1-pentyl-1H-benzimidazol-2-yl)benzene scaffold is T-shaped, resulting from the coordination of Se by the C atom of the central aromatic ring and the N atoms of both of the benzimidazole moieties. ThetransSe—N bond lengths are almost equal [2.087 (3) and 2.099 (3) Å

APA, Harvard, Vancouver, ISO, and other styles

48

Wei, Tai-Bao, Yan-Yun Lu, Cheng Cao, Hong Yao, and You-Ming Zhang. "1-[2,2-Bis(1,3-benzimidazol-1-ylmethyl)-3-bromopropyl]-1,3-benzimidazole." Acta Crystallographica Section E Structure Reports Online 67, no. 7 (2011): o1833. http://dx.doi.org/10.1107/s1600536811023464.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Ennajih, Hamid, Rachid Bouhfid, El Mokhtar Essassi, and Seik Weng Ng. "2-[3-(1H-Benzimidazol-2-yl)propyl]-1-decyl-1H-benzimidazole." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2544. http://dx.doi.org/10.1107/s160053681103501x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Nguyen Tien, Cong, Duc Tran Thi Cam, Ha Bui Manh, and Dat Nguyen Dang. "Synthesis and Antibacterial Activity of Some Derivatives of 2-Methylbenzimidazole Containing 1,3,4-Oxadiazole or 1,2,4-Triazole Heterocycle." Journal of Chemistry 2016 (2016): 1–6. http://dx.doi.org/10.1155/2016/1507049.

Full text

Abstract:

5-[(2-Methyl-1H-benzimidazol-1-yl)methyl]-1,3,4-oxadiazole-2-thiol or 5-[(2-methyl-1H-benzimidazol-1-yl)methyl]-4-(4-methylphenyl)-1,2,4-triazol-3-thiol which were prepared starting from 2-methylbenzimidazole in the reaction with appropriateN-aryl-2-chloroacetamides afforded two series ofN-aryl-2-{5-[(2-methyl-1H-benzimidazol-1-yl)methyl]-1,3,4-oxadiazol-2-yl}sulfanylacetamides andN-aryl-2-{5-[(2-methyl-1H-benzimidazol-1-yl)methyl]-4-(4-methylphenyl)-4H-1,2,4-triazol-3-ylthio}acetamides, respectively. The structures of the compounds were elucidated on the basis of IR, MS,1H-NMR, and13C-NMR spe

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!