Relevant bibliographies by topics / 4-(N-phenylcarbamoyl) butanoic acid

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Academic literature on the topic '4-(N-phenylcarbamoyl) butanoic acid'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "4-(N-phenylcarbamoyl) butanoic acid"

1

R., S. Dhivare, and S. Rajput S. "Synthesis, Characterization and Antimicrobial Evolution of Six Membered Cyclic Imides." International Journal of Chemistry and Pharmaceutical Sciences 3, no. 8 (2015): 1877–80. https://doi.org/10.5281/zenodo.3909339.

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A B S T R A C T The six-membered cyclic imide derivatives were synthesized by reacting glutaric anhydride with different substituted aromatic amines to get 4-(N-phenyl carbamoyl) butanoic acid. These intermediates underwent ring closer with acetyl chloride furnished six-membered cyclic imides derivatives. All these derivatives were screened for antimicrobial activities.
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2

Hanifa, Bibi, Muhammad Sirajuddin, Ahmed Bari, See Mun Lee, Kong Mun Lo, and Edward R. T. Tiekink. "4-[(4-Chlorophenyl)carbamoyl]butanoic Acid." Molbank 2021, no. 2 (2021): M1209. http://dx.doi.org/10.3390/m1209.

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The X-ray crystal structure determination of the glutaric acid-amide derivative, 4-ClC6H4N(H)C(=O)(CH2)3C(=O)OH (1), is described. The backbone of the molecule adopts an extended, all-trans configuration but the terminal carboxylic acid and phenyl resides are twisted out of the plane through the bridging atoms, as seen in the torsion angles of O(carboxylic acid)–C(m)–C(m)–C(m) [13.9(5)°] and C(m)–N–C(p)–C(p) [47.1(4)°]; m = methylene and p = phenyl. The most striking feature of the molecular packing is the formation of supramolecular tapes mediated by carboxylic acid-O–H⋯O(carbonyl) and amide-
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3

Hanifa, Bibi, Muhammad Sirajuddin, Zafran Ullah, et al. "4-[(2,4-Dichlorophenyl)carbamoyl]butanoic Acid." Molbank 2021, no. 2 (2021): M1227. http://dx.doi.org/10.3390/m1227.

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The synthesis and spectroscopic characterization of the glutaric acid-amide derivative, 2,4-Cl2C6H3N(H)C(=O)(CH2)3C(=O)OH (1), are described. The X-ray crystal structure determination of (1) shows the backbone of the molecule to be kinked about the methylene-C–N(amide) bond as seen in the C(p)–N–C(m)–C(m) torsion angle of −157.0(2)°; m = methylene and p = phenyl. An additional twist in the molecule is noted between the amide and phenyl groups as reflected in the C(m)–N–C(p)–C(p) torsion angle of 138.2(2)°. The most prominent feature of the molecular packing is the formation of supramolecular t
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4

VORONKOV, M. G., B. SHIRCHIN, V. YU VVEDENSKII, and P. AD'YAASUREN. "ChemInform Abstract: 4-(N,N-Dimethylamino)butanoic Acid Triorganylsilylmethyl Esters." ChemInform 24, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199329185.

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5

David, Y. C., J. B. Ylagan, H. A. Gonzales, et al. "Volatile organic compound profiling of Capsicum annuum var. longum grown under different concentrations of nitrogen." Hellenic Plant Protection Journal 14, no. 2 (2021): 77–88. http://dx.doi.org/10.2478/hppj-2021-0008.

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Summary Emission of volatile organic compounds (VOCs) in plants is triggered by several biotic and abiotic factors, such as nutrient deficiency, environmental stress, and pathogenic attacks. For instance, plants suffering from limited or excessive nitrogen (N) supply may experience internal stress which can ultimately lower their stability and immunity making them susceptible to infection and infestation. In this study, VOCs from Capsicum annuum var. longum (Solanaceae) exposed to nitrogen (1.8 g/L, 4.5 g/L, and 9 g/L urea) were extracted using a 100 μm Solid Phase Microextraction (SPME) fiber
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6

Otogawa, Kohei, Kazuhiko Ishikawa, Motoo Shiro, and Toru Asahi. "Crystal structure of (S)-4-carbamoyl-4-(1,3-dioxoisoindolin-2-yl)butanoic acid." Acta Crystallographica Section E Crystallographic Communications 71, no. 1 (2015): 107–9. http://dx.doi.org/10.1107/s2056989014027121.

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In the title compound, C13H12N2O5, the phthalimide ring system is essentially planar, with a maximum deviation of 0.0479 (14) Å. In the crystal, each molecule is linkedviasix neighbouring molecules into a three-dimensional network through N—H...O and O—H...O hydrogen bonds, which form anR32(8) ring motif.
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7

Jędrzejczak, Karol, Małgorzata Szczesio, Monika Oracz, Stefan Jankowski, and Marek L. Główka. "Crystal structure of (3R)-3-benzyl-4-[(tert-butoxycarbonyl)amino]butanoic acid." Acta Crystallographica Section E Structure Reports Online 70, no. 10 (2014): o1081—o1082. http://dx.doi.org/10.1107/s1600536814019497.

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The characteristic feature of the title molecule, C16H23NO4, is thesynconfiguration of the partially double amide C—N bond [C—N—C—O torsion angle = −14.8 (2)°]. The crystal packing is determined by intermolecular O—H...O and N—H...O hydrogen bonds, which link the molecules into a double-chain structure extending along [010].
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8

Nazir, Majid, Muhammad Athar Abbasi, Aziz-ur-Rehman Aziz-ur-Rehman, et al. "Novel indole based hybrid oxadiazole scaffolds with N-(substituted-phenyl)butanamides: synthesis, lineweaver–burk plot evaluation and binding analysis of potent urease inhibitors." RSC Advances 8, no. 46 (2018): 25920–31. http://dx.doi.org/10.1039/c8ra04987d.

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In the study presented herein, 4-(1H-indol-3-yl)butanoic acid (1) was sequentially transformed in the first phase into ethyl 4-(1H-indol-3-yl)butanoate (2), 4-(1H-indol-3-yl)butanohydrazide (3) and 5-[3-(1H-indol-3-yl)propyl]-1,3,4-oxadiazole-2-thiol (4) as a nucleophile.
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9

Kumar, Ranjan, and Ajendra Kumar. "Experiment of Kinetics Oxidation of Substituted 3'-4'-Dimethylphenyl by N-chlorosaticarin in Acetic-acid Reaction." Journal of Advances in Science and Technology 22, no. 1 (2025): 8–14. https://doi.org/10.29070/3razbr88.

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The oxidation process of 3'-4'-dimethylphenyl time and butanoic acid using N-chlorosaccharin in an acetic acid medium, with perhydrochloric acid as a catalyst, was investigated. The reaction followed a primary order with respect to [ka], [NCSA], and [H+]. The sole oxidation product identified was 3,4-dimethylbenzoic acid. To regulate the reaction rate involving the acid and its products, saccharin formed as a byproduct was introduced. The dissociation of ionic forces within the reaction site had minimal influence on oxidation speed across various conditions. However, a slight reduction in the
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Jawad Kadhim, Abdullah, та Ali Chazi Kazim. "Synthesis and Characterization of Benzimidazole by Using o-Phenylenediamine with Different Aldehydes and Carboxylic Acids in the Presence of ρ-TSOH as a Catalyst". Oriental Journal of Chemistry 34, № 4 (2018): 2131–36. http://dx.doi.org/10.13005/ojc/3404054.

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This research paper deals with the synthesis and diagnose of Benzimidazole rings which were have been prepared by using two different methods in which used starting material o-phenylenediamine with different compounds. The first method is with aldehydes such as 4-Chlorobenzaldehyde, 4-N, N-Dimethylbenzaldehyde, and Formaldehyde. The second is with Carboxylic acids such as Salicylic acid, Acetic acid, and Butanoic acid. ρ-TSOH has been using as a catalyst in the synthesis methods above and used F.T.I.R and HNMR spectroscopy are used for diagnosing the prepared rings in addition to the physical
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Conference papers on the topic "4-(N-phenylcarbamoyl) butanoic acid"

1

Muinos, Martin, Spencer Harp, Benoit Kindo, Remi Gaubert, and Valentin Soloiu. "Combustion and Emissions Characteristics of a Brassica Carinata FAME and N-Butanol Blend." In ASME 2016 Power Conference collocated with the ASME 2016 10th International Conference on Energy Sustainability and the ASME 2016 14th International Conference on Fuel Cell Science, Engineering and Technology. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/power2016-59397.

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In this study, the combustion and emissions characteristics of a new biodiesel and biodiesel blend in a direct injection (DI), experimental diesel engine and was compared to ultra-low sulfur diesel #2 (ULSD#2) at 1500 rpm and 4 bar indicated mean effective pressure (IMEP). The biodiesel blend, C90+BU10, included 90% brassica carinata (25% erucic acid methyl ester) and 10% n-butanol bio-alcohol by mass. The lower heating value of C90+BU10 was 37.25 MJ/kg, compared to 42.6 MJ/kg for ULSD#2. The ignition delay of ULSD#2 was 9.0 crank angle degrees (CAD) and decreased to 8.5 CAD for C90+BU10, whic
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