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Relevant bibliographies by topics / Chlorobenzamidine

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Academic literature on the topic 'Chlorobenzamidine'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Chlorobenzamidine"

1

Chandrakar, Lalta Prasad, Raghunandan Singh, and Rajendrakumar Mishra. "Extraction-spectrophotometric determination of molybdenum with N-m-tolyl-N′-p-chlorophenyl-o-chlorobenzamidine hydrochloride and thiocyanate." Analyst 112, no. 11 (1987): 1511–13. http://dx.doi.org/10.1039/an9871201511.

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2

L., P. CHANDRAKAR, and K. MISHRA R. "Extractive Spectrophotometric Determination of Molybdenum(v) with N-Hydroxy-N-p-chlorophenyl-N'-p-chlorophenyl-o-chlorobenzamidine Hydrochloride in Presence of Thiocyanate." Journal of Indian Chemical Society Vol. 63, Oct 1986 (1986): 920–22. https://doi.org/10.5281/zenodo.6302337.

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D. B. Science College, Gondia (M. B.) Department of Chemistry, Ravishankar University, Raipur-492 010 <em>Manuscript </em>received 12 March <em>2986, </em>revised <em>29 July </em>1986, <em>accepted 23 August 1986</em> A new spectrophotometric method for the determination of molybdenum(v) at ppm level has been developed. The newly synthesised reagent <em>N</em>-hydroxy-<em>N</em>-<em>p</em>-cldorophenyl-<em>N</em>'-<em>p</em>-chlorophenyl-<em>o</em>-chlorobenzamidine hydrochloride has been used as a chelating agent, and ascorbic acid as a reducing agent for reducing M<sup>VI</sup>&nbs

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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

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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5

Xing, Zhi-Tao, Wei-Lin Ding, Hai-Bo Wang, Jun Yin, and Feng Han. "2-Chlorobenzamide oxime monohydrate." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (2007): o1019—o1020. http://dx.doi.org/10.1107/s1600536807004114.

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6

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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7

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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8

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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9

Qingxiang, Zhou, Lu Wenying, Liu Guoguang, and Xue Xiuling. "Study on the Hydrolysis of 2-Chlorobenzamide." Journal of Agricultural and Food Chemistry 48, no. 6 (2000): 2572–75. http://dx.doi.org/10.1021/jf990163a.

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10

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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Book chapters on the topic "Chlorobenzamidine"

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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