Relevant bibliographies by topics / Chlorobenzamido

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Academic literature on the topic 'Chlorobenzamido'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Chlorobenzamido"

1

Hasana, Ani Riani, Siswandono Siswandono, and Marcellino Rudyanto. "Synthesis and characterization of 2-Benzamido-NBenzylbenzamide Derivative." JURNAL ILMU KEFARMASIAN INDONESIA 20, no. 2 (2022): 281. http://dx.doi.org/10.35814/jifi.v20i2.1135.

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Anthranilamide derivatives exhibit anti-inflammatory, antipyretic, antibacterial, antiangiogenic, and anticoagulant properties. With an early in silico examination of its analgesic capabilities, this study aimed to generate a novel anthranilamide molecule by altering 2-Benzamido-N-Benzylbenzamide. Modification of anthranilamide with 1/2/3-chloro benzoyl chloride by acylation resulted in the design, synthesis, characterization, and research of the analgesic effects of 2-benzamido-N-benzoylbenzamide derivatives. 2-(2-chlorobenzamido)-N-(2-chlorobenzoyl)benzamide, 2-(3-chlorobenzamido)-N-(3-chlor
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2

Yadav, Bishwa Nath, Shambhu Prasad, and Satya Murti Prasad. "Methyl 2-(2-chlorobenzamido)benzoate." Acta Crystallographica Section E Structure Reports Online 58, no. 11 (2002): o1198—o1199. http://dx.doi.org/10.1107/s160053680201807x.

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Khan, Islam Ullah, Onur Şahin, Rashid Javaid, Shahzad Sharif, and Orhan Büyükgüngör. "Methyl 2-(4-chlorobenzamido)benzoate." Acta Crystallographica Section E Structure Reports Online 66, no. 12 (2010): o3338. http://dx.doi.org/10.1107/s160053681004897x.

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4

Ouahrouch, Abdelaaziz, Moha Taourirte, Hassan B. Lazrek, Mohamed El Azhari, Mohamed Saadi, and Lahcen El Ammari. "Methyl 2-(3-chlorobenzamido)benzoate." Acta Crystallographica Section E Structure Reports Online 68, no. 12 (2012): o3400—o3401. http://dx.doi.org/10.1107/s1600536812046934.

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Breznica-Selmani, Pranvera, Kristina Mladenovska, Zoran Kavrakovski, Bozhana Mikhova, Gerald Draeger, and Emil Popovski. "[(3-Chlorobenzamido)methyl]triethylammonium Chloride." Molbank 2015, no. 2 (2015): M851. http://dx.doi.org/10.3390/m851.

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Khan, Zulfiqar Ali, Khalid M. Khan, and Shazia Anjum. "2-(2-Chlorobenzamido)benzoic acid." Acta Crystallographica Section E Structure Reports Online 63, no. 10 (2007): o4103. http://dx.doi.org/10.1107/s1600536807044352.

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Khan, Islam Ullah, Muneeb Hayat Khan, Muhammad Nadeem Arshad, and Mehmet Akkurt. "2-(4-Chlorobenzamido)acetic acid." Acta Crystallographica Section E Structure Reports Online 67, no. 4 (2011): o916. http://dx.doi.org/10.1107/s1600536811009536.

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8

Brandy, Yakini, Ray J. Butcher, Tolulope A. Adesiyun, Solomon Berhe, and Oladapo Bakare. "2-Chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone." Acta Crystallographica Section E Structure Reports Online 65, no. 1 (2008): o64. http://dx.doi.org/10.1107/s1600536808040993.

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9

Moreno-Fuquen, Rodolfo, Vanessa Melo, and Javier Ellena. "Crystal structure of 2-(4-chlorobenzamido)benzoic acid." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (2015): o856—o857. http://dx.doi.org/10.1107/s2056989015017879.

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In the title molecule, C14H10ClNO3, the amide C=O bond isantito theo-carboxy substituent in the adjacent benzene ring, a conformation that facilitates the formation of an intramolecular amide-N—H...O(carbonyl) hydrogen bond that closes anS(6) loop. The central amide segment is twisted away from the carboxy- and chloro-substituted benzene rings by 13.93 (17) and 15.26 (15)°, respectively. The most prominent supramolecular interactions in the crystal packing are carboxylic acid-H...O(carboxyl) hydrogen bonds that lead to centrosymmetric dimeric aggregates connected by eight-membered {...HOC=O}2s
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10

M., M. DUTTA, N. GOSWAMI B., and C. S. KATAKY J. "Studies on Biologically Active Heterocycles. Part-III. Synthesis and Antibacterial Activity of some 2-Aryl/ Aralkyl-3-substituted-4-thiazolidinones." Journal of Indian Chemical Society Vol. 67, April 1990 (1990): 332–34. https://doi.org/10.5281/zenodo.6163457.

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Regional Research Laboratory, Jorhat-785 006 <em>Manuscript received 30 January 1989, revised 24 July 1989, accepted 21 November 1989</em> A series of new 2-aryl/aralkyl-3-[2,4&middot;dichlorobenzamido]-4-thiazolidinones and 2-aryl/aralkyl-3-[2-chlorobenzamido]-4-thiazolidinones have been synthesised by con- densation of the respective hydrazones with&nbsp;mercaptoacetic acid. The hydrazones have been prepared by condensing different aromatic and aliphatic aldehydes with the corresponding acylhydrazides. All the compounds were screened for their antibacterial activity.
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Book chapters on the topic "Chlorobenzamido"

1

Mullan, E. L., and C. H. Williams. "Kinetics of inhibition of MAO-B by N-(2-aminoethyl)-p-chlorobenzamide (Ro 16-6491) and analogues." In Amine Oxidases: Function and Dysfunction. Springer Vienna, 1994. http://dx.doi.org/10.1007/978-3-7091-9324-2_40.

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