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Relevant bibliographies by topics / N-chlorobenzamide

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Academic literature on the topic 'N-chlorobenzamide'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "N-chlorobenzamide"

1

Saeed, Aamer, Rasheed Ahmad Khera, Naeem Abbas, Jim Simpson, and Roderick G. Stanley. "N-Butyl-4-chlorobenzamide." Acta Crystallographica Section E Structure Reports Online 64, no. 12 (2008): o2322—o2323. http://dx.doi.org/10.1107/s1600536808036313.

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2

Zheng, Xi, Bo Li, Qiang Wang, and Li Guo. "N-Benzylcarbamothioyl-2-chlorobenzamide." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1774. http://dx.doi.org/10.1107/s1600536810023822.

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3

Wisnu, Elok Dea Orens Ubung, Indah Purnama Sary, and Dwi Koko Pratoko. "Sintesis dan Uji Aktivitas Antibakteri Senyawa N-fenil-4-klorobenzamida." Pustaka Kesehatan 6, no. 2 (2018): 212. http://dx.doi.org/10.19184/pk.v6i2.7569.

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N-phenylbenzamide is benzamide derivatives, which is potential as an antibacterial agent. N-phenyl-4-chlorobenzamide is N-phenylbenzamide derivative that substitued by chloro to the para position and it was expected to enhance the antibacterial activity. N-phenyl-4-chlorobenzamide was synthesized by reacting 1,3-diphenyilthiourea and 4-chlorobenzoil chloride. This compound has been purified and provided 53% of product with crystal shape, white color, and melting point of 195-197 oC. The purification of this compound was confirmed by TLC and the structure was identified by 1H-NMR, 13C-NMR, and

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4

Khawar Rauf, M., Michael Bolte, and Amin Badshah. "N-(Benzothiazol-2-yl)-3-chlorobenzamide." Acta Crystallographica Section E Structure Reports Online 65, no. 6 (2009): o1245. http://dx.doi.org/10.1107/s1600536809016481.

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The title molecule, C14H9ClN2OS, exists in the solid state in its amide form with a typical C=O bond length, as well as shortened C—N bonds. The plane containing the HNCO atoms subtends dihedral angles of 12.3 (4) and 8.1 (3)° with the planes of the phenyl ring and benzothiazole group, respectively, whereas the dihedral angle between the planes of the phenyl ring and the benzothiazole group is 5.96 (6)°. In the crystal, molecules form intermolecular N—H...N hydrogen bonds, generating independent scissor-likeR22(8) dimers.

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5

Ghare, Sakshi. "Synthesis of 2-chloro-benzamides for evaluation antimicrobial and disinfectant activity: Part-I." Current Trends in Pharmacy and Pharmaceutical Chemistry 6, no. 1 (2024): 26–27. http://dx.doi.org/10.18231/j.ctppc.2024.009.

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2-Chlorobenzamide derivatives have been synthesized and claimed in this research study. The compound SG1 and SG2 were synthesized by known methods Ethylene diamine and isopropyl amine was dissolved in ethanolic 1 N NaOH separately and to it 2-Chlorobenzoyl chloride was added. The products SG1 and SG2 were collected respectively.

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6

B., Thimme Gowda, C. Mary M., and Jyothi K. "Kinetics and mechanism of oxidation of thiosemicarbazide by substituted-N-chlorobenzamides in aqueous methanol medium." Journal of Indian Chemical Society Vol. 78, Aug 2001 (2001): 407–11. https://doi.org/10.5281/zenodo.5878491.

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Department of Post-Graduate Studies and Research in Chemistry, Mangalore University, Mangalagangothri-574 199, India <em>E-mail</em> : gowdabt@yahoo.com  <em> Fax </em>: 91-824-7423671742424 Manuscript received 18 October 2000, accepted 22 March 2001 The kinetics of oxidation of thiosemicarbazide by <em>N</em>-chlorobenzamide, <em>N</em>-chloro-<em>p</em>-methyl-, <em>N</em>-chloro-<em>p</em>-chloro- and <em>N</em>-chloro-<em>p</em>-nitrobenzamides have been studied in aqueous methanol in the presence of perchloric acid. The reactions show first order kinetics in [oxidant], fractiona

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7

Sow, Salif, Felix Odame, Ngoné Diouf, et al. "Syntheses and X-ray Structure of N-(Benzothiazol-2-yl)-3-chlorobenzamide." International Research Journal of Pure and Applied Chemistry 25, no. 4 (2024): 1–9. http://dx.doi.org/10.9734/irjpac/2024/v25i4861.

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The reaction of 3-chloro-benzoyl chloride and 2-aminobenzothiazole in the presence of potassium thiocyanate yielded a yellowish solid C15H10ClN3OS2 (1). Reaction of 1 with cobalt chloride yield a yellowish solid C14H11ClN2O2S (2) which gives crystal suitable for X-ray analyses. The compounds were characterized by elemental analyses FTIR spectroscopy and melting point measurement. Compound 2 crystallizes in the triclinic space group Pī with the following parameters: a = 7.0299(2) Å b = 7.0466(2) Å c = 14.5490(2) Å a = 103.844(3)° β = 92.929(2)° g = 107.291(3) V = 662.33(4) Å3 Z= 2 R1 = 0.030 wR

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8

COŞMAN, Sertaç. "Experimental Research of the Effects of Benzoylthiourea Derivative Fuel and Gasoline Mixtures on Engine Performance and Emissions." International Journal of Automotive Science and Technology 7, no. 4 (2023): 403–9. http://dx.doi.org/10.30939/ijastech..1397506.

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In this study, the influences of Benzoylthiourea Derivative Fuel N-(2-amino-5-bromo-1,dihydropyridine-1-yl)carbonothioyl)-2-chlorobenzamide as an additive into gas-oline were researched on engine performance and exhaust emissions. For this reason, a single-cylinder four stroke gasoline engine was run at wide open throttle, and 2400, 2800, 3200, 3600 and 4000 rpm engine speeds. The changes of engine torque, power output, specific fuel consumption, thermal efficiency, CO, CO2 and HC emissions were experi-mentally investigated.

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9

Skibiński, Robert, and Łukasz Komsta. "Application of Curve Resolution Algorithms in the Study Drug Photodegradation Kinetics—The Example of Moclobemide." Journal of AOAC INTERNATIONAL 95, no. 3 (2012): 708–12. http://dx.doi.org/10.5740/jaoacint.sge_skibinski.

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Abstract The photodegradation of moclobemide was studied in methanolic media. Ultra-HPLC (UHPLC)/MS/MS analysis proved decomposition to 4-chlorobenzamide as a major degradation product and small amounts of Ro 16-3177 (4-chloro-N-[2-[(2-hydroxyethyl)amino] ethyl]benzamide) and 2-[(4-chlorobenzylidene)amino]-N-[2-ethoxyethenyl]ethenamine. The methanolic solution was investigated spectrophotometrically in the UV region, registering the spectra during 30 min of degradation. Using reference spectra and a multivariate chemometric method (multi- variate curve resolution-alternating least squares), th

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10

M. Salih, Kezhal, and Hashim J. Azeez. "Synthesis and Spectral Characterization of a New Series of N-4-Chlorobenzamide-5- phenylthiazolidin-3-one." Rafidain Journal of Science 27, no. 1 (2018): 15–28. http://dx.doi.org/10.33899/rjs.2018.141182.

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Book chapters on the topic "N-chlorobenzamide"

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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