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Relevant bibliographies by topics / Carbothioamide

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Academic literature on the topic 'Carbothioamide'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Carbothioamide"

1

Nayak, Riddhi A., and Anvita D. Mangte. "Synthesis and Antimicrobial Studies of Novel N-Glycosyl Hydrazino Carbothioamide." Asian Journal of Chemistry 33, no. 1 (2020): 127–31. http://dx.doi.org/10.14233/ajchem.2021.22967.

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In view of applications of N-glycosylated compounds in medicinal chemistry and in many other ways, herein the synthesis of novel N-glycosyl hydrazino carbothioamides is reported. New N-glycosyl hydrazino carbothioamides were synthesized by the condensation of per-O-acetyl glycosyl isothiocyanate with different aromatic hydrazides. The newly synthesized compounds were characterized by using the IR, 1H NMR and mass spectral studies. Antimicrobial evaluation of the synthesized N-glycosyl hydrazino carbothioamide was also examined. Antimicrobial activities of the synthesized compound were evaluate

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M. Younis, Norhan, Amr M. Abdelghany, Fathy Shaaban, Tamer K. Khatab, Ehab Abdel-Latif, and Heba M. Metwally. "Zeolite A/ZnCl2 nanoparticles as a catalyst for eco-friendly synthesis of pyrazole-1- carbothioamides with docking validation as Covid-19 main protease (MPRO) inhibitor." Bulletin of the Chemical Society of Ethiopia 37, no. 2 (2022): 391–404. http://dx.doi.org/10.4314/bcse.v37i2.11.

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ABSTRACT. The synthesized Zeolite A/ZnCl2 nanoparticles via the hydrothermal route were characterized using FTIR, XRD, and SEM/EDAX techniques. The characterized catalyst was used for the eco-friendly synthesis of 4,5-dihydro-pyrazole-1-carbothioamide derivatives. Under solvent-free conditions, a multi-component reaction between hydrazine, isothiocyanate, and chalcone was done with a prepared nano-catalyst as an inexpensive, recyclable, easy-to-get, and nontoxic catalyst. The molecular docking study explained that dihydro-1-carbothioamide pyrazoles can be considered COVID-19 main protease (Mpr

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3

Shaibah, Mohammed A. E., Hemmige S. Yathirajan, Asma, et al. "Conversion of diarylchalcones into 4,5-dihydropyrazole-1-carbothioamides: molecular and supramolecular structures of two precursors and three products." Acta Crystallographica Section E Crystallographic Communications 76, no. 3 (2020): 360–65. http://dx.doi.org/10.1107/s2056989020001735.

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Chalcones of type 4-XC6H4C(O)CH=CHC6H4(OCH2CCH)-4, where X = Cl, Br or MeO, have been converted to the corresponding 4,5-dihydropyrazole-1-carbothioamides using a cyclocondensation reaction with thiosemicarbazide. The chalcones 1-(4-chlorophenyl)-3-[4-(prop-2-ynyloxy)phenyl]prop-2-en-1-one, C18H13ClO2, (I), and 1-(4-bromophenyl)-3-[4-(prop-2-ynyloxy)phenyl]prop-2-en-1-one, C18H13BrO2, (II), are isomorphous, and their molecules are linked into sheets by two independent C—H...π(arene) interactions, both involving the same aryl ring with one C—H donor approaching each face. In each of the product

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4

Castiñeiras, Alfonso, Nuria Fernández-Hermida, Isabel García-Santos, and Lourdes Gómez-Rodríguez. "Synthesis and Characterization of Some 5-Acetylbarbituric Based Thiosemicarbazone Derivatives." Proceedings 41, no. 1 (2019): 10. http://dx.doi.org/10.3390/ecsoc-23-06479.

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A new series of 5-acetylbarbituric based thiosemicarbazones named 5-acetylbarbituric hydrazine-1-carbothioamide (Acb4NDH, 1), N-methyl-(5-acetylbarbituric)hydrazine- 1-carbothioamide (Acb4NM, 2), N-ethyl-(5-acetylbarbituric)hydrazine-1-carbothioamide (Acb4NE, 3), N,N-dimethyl-(5-acetylbarbituric)hydrazine-1-carbothioamide (Acb4NDM, 4), N′-piperidine- (5-acetylbarbituric)-1-carbothiohydrazide (Acb4Npip, 5) and N′-hexamethyleneimine- (5-acetylbarbituric)-1-carbothiohydrazide (Acb4Nhexim, 6), has been synthesized from 5-acetylbarbituric acid and N-unsubstituted/substituted thiosemicarbazides. The

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5

Tarai, Arup, and Jubaraj Bikash Baruah. "Separation or combination of non-covalently linked partners provides polymorphs of N-(aryl)-2-(propan-2-ylidene)hydrazine carbothioamides." CrystEngComm 21, no. 9 (2019): 1397–406. http://dx.doi.org/10.1039/c8ce02000k.

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6

Neumann, Tristan, Inke Jess та Christian Näther. "Crystal structure ofcatena-poly[[[bis(pyridine-4-carbothioamide-κN1)cadmium]-di-μ-thiocyanato-κ2N:S;κ2S:N] methanol disolvate]". Acta Crystallographica Section E Crystallographic Communications 72, № 3 (2016): 370–73. http://dx.doi.org/10.1107/s2056989016002632.

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The asymmetric unit of the polymeric title compound, {[Cd(NCS)2(C6H6N2S)]·2CH3OH}n, consists of one cadmium(II) cation that is located on a centre of inversion as well as one thiocyanate anion, one pyridine-4-carbothioamide ligand and one methanol molecule in general positions. The CdIIcations are octahedrally coordinated by the pyridine N atom of two pyridine-4-carbothioamide ligands and by the S and N atoms of four thiocyanate anions and are linked into chains along [010] by pairs of anionic ligands. These chains are further linked into layers extending along (201) by intermolecular N—H...O

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Neumann, Tristan, Inke Jess та Christian Näther. "Crystal structure of bis(pyridine-4-carbothioamide-κN1)bis(thiocyanato-κN)cobalt(II) methanol monosolvate". Acta Crystallographica Section E Crystallographic Communications 73, № 11 (2017): 1786–89. http://dx.doi.org/10.1107/s2056989017015055.

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The asymmetric unit of the title compound, [Co(NCS)2(C6H6NS)4]·CH3OH, consists of one cobalt(II) cation, two thiocyanate anions, four pyridine-4-carbothioamide ligands and one methanol molecule that are located in general positions. The CoIIcations are coordinated by two terminal N-bonding thiocyanate anions and four N-bonding pyridine-4-carbothioamide ligands, resulting in discrete and slightly distorted octahedral complexes. These complexes are linked into a three-dimensional networkviaintermolecular N—H...S hydrogen bonding between the amino H atoms and the thiocyanate and pyridine-4-carbot

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8

Li, Yu-Feng, and Fang-Fang Jian. "N-Phenylpiperidine-1-carbothioamide." Acta Crystallographica Section E Structure Reports Online 64, no. 9 (2008): o1743. http://dx.doi.org/10.1107/s1600536808025142.

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9

Li, Yu-Feng. "N-Cyclohexylpyrrolidine-1-carbothioamide." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (2012): o1220. http://dx.doi.org/10.1107/s1600536812012627.

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In the title molecule, C11H20N2S, the five-membered ring has an envelope conformation and the cyclohexane ring is in a chair conformation. The N—H group is not involved in any intra- or intermolecular interactions.

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Umar, M. Naveed, M. Nawaz Tahir, Mohammad Shoaib, Akbar Ali, and Imran Khan. "N-Methylpyrrolidine-1-carbothioamide." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (2012): o1706. http://dx.doi.org/10.1107/s1600536812020971.

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There are two independent molecules in the asymmetric unit of the title compound, C6H12N2S, in which the N-methylthioformamide unit and the pyrrolidine ring mean plane are oriented at dihedral angles of 5.9 (5) and 5.9 (4)°. In the crystal, zigzag C(4) chains extending along the a axis are formed due to N—H...S hydrogen bonds between alternate arrangements of molecules. The chains are interlinked by C—H...S hydrogen bonds.

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Book chapters on the topic "Carbothioamide"

1

Franchetti, P., E. Nasini, S. Vittori, E. Lepri, G. Nocentini, and A. Barzi. "Antitumor Activity of Metal(II) Chelates of 2,2′-Bipyridyl-6-Carbothioamide: in Vitro Study." In Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1717-3_72.

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Ferkous, Hana, Souad Djellali, Rachid Sahraoui, Hamza Behloul, Khaoula Saoud, and Alaaddin Çukurovali. "2-(2-Methoxybenzylidene) Hydrazine-1-Carbothioamide as Efficient Organic Inhibitor for Mild Steel in Hydrochloric Acid Solution." In Recent Advances in Environmental Science from the Euro-Mediterranean and Surrounding Regions (2nd Edition). Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-51210-1_235.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand complex of cobalt(II) with [(methylthiophen-2-yl)methylene]hydrazono-carbothioamide and thiocyanate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_556.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand complex of cobalt(II) with [(methylthiophen-2-yl)methylene]hydrazono-carbothioamide and cyanate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_557.

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5

Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand complex of copper(II) with [(methylthiophen-2-yl)methylene]hydrazono-carbothioamide and thiocyanate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_261.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand complex of copper(II) with [(methylthiophen-2-yl)methylene]hydrazono-carbothioamide and cyanate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_262.

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7

Pardasani, R. T., and P. Pardasani. "Magnetic properties of chromium(III) complex with 3-methyl-5-oxo-N,1-diphenyl-4,5-dihydro-1-H-pyrazol-4-carbothioamide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_31.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) complex with 3-methyl-5-oxo-N,1-diphenyl-4,5-dihydro-1-H-pyrazol-4-carbothioamide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_129.

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9

Ferkous, Hana, Souad Djellali, Rachid Sahraoui, Hamza Behloul, Khaoula Saoud, and Alaaddin Çukurovali. "Electrochemical Impedance Spectroscopy and Adsorption Study of Carbon Steel in 1 M HCl Solution Containing 2-(2-Methoxybenzylidene) Hydrazine-1-Carbothioamide." In Recent Advances in Environmental Science from the Euro-Mediterranean and Surrounding Regions (2nd Edition). Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-51210-1_9.

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10

Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear cobalt(II) complex with 3-methyl-5-oxo-N,1-diphenyl-4,5-dihydro-1-H-pyrazol-4-carbothioamide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_225.

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Conference papers on the topic "Carbothioamide"

1

Wang, Qinqin, Yuping Guo, Min Wang, WuFu Zhu, and Shan Xu. "Synthesis of 3-bromo-4-isobutyloxyphenyl carbothioamide." In 2015 2nd International Conference on Machinery, Materials Engineering, Chemical Engineering and Biotechnology. Atlantis Press, 2016. http://dx.doi.org/10.2991/mmeceb-15.2016.157.

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2

Guliyeva, Lala, Muhammed Trawally, Kübra Demir-Yazıcı, Kerem Kaya, Atilla Akdemir, and Özlen Güzel-Akdemir. "Thione or Thiol: Sructural Confirmation of (E)-2-(1-(4-cyanophenyl)ethylidene)-N-(2-fluoro-4-sulfamoylphenyl)hydrazine-1-Carbothioamide and Carbonic Anhydrase Inhibition Studies." In 8th International Students Science Congress. ULUSLARARASI ÖĞRENCİ DERNEKLERİ FEDERASYONU (UDEF), 2024. https://doi.org/10.52460/issc.2024.060.

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Thiosemicarbazones are Schiff bases formed by condensing an aldehyde or ketone with thiosemicarbazide derivatives. TSCs exhibit various biological activities and act as precursors for key scaffolds, with keto-enol tautomerism commonly resulting in thione or thiol forms. This study focuses on synthesizing and confirming the structure of compound 1, (E)-2-(1-(4-cyanophenyl)ethylidene)-N-(2-fluoro-4-sulfamoylphenyl)hydrazine-1-carbothioamide, through a condensation reaction in methanol. Both theoretical and experimental IR and X-ray studies confirm the presence of the thione form and E isomerism.

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Ledeneva, Irina, Vitaly Didenko, Victor Dotsenko, and Khidmet Shikhaliev. "Synthesis and reactions of pyrazolo[5,1-c][1,2,4]triazine-3-carbothioamides." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a040.

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Miletin, Miroslav, Jiri Hartl, Martin Dolezal, Zelmira Odlerova, Katarina Kralova, and Milos Machacek. "Synthesis of Some 2,6-Disubstituted 4-Pyridinecarboxamides and -Carbothioamides, and Their Antimycobacterial and Photosynthesis-Inhibiting Activity." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01695.

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Nagarjuna, Ummadi, Gundala Sravya, S. Durgamma, Adivireddy Padmaja, and Grigory V. Zyryanov. "Synthesis of a new class of heteroaryl dipyrazolyl carbothioamides and heteroaryl dipyrazolyl thiazoles and evaluation as antioxidants." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087371.

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