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N-(2-chlorophenyl)-2-hydroxybenzamide is a chemical compound with the molecular formula C13H9ClNO2. It is a derivative of benzamide, featuring a 2-chlorophenyl group attached to the nitrogen atom and a hydroxyl group on the benzene ring. N-(2-chlorophenyl)-2-hydroxybenzamide is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a precursor in the synthesis of various biologically active molecules. Its structure allows for the exploration of different chemical properties and reactivity patterns, making it a subject of interest in organic chemistry research.

1697-18-3

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1697-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1697-18-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1697-18:
(6*1)+(5*6)+(4*9)+(3*7)+(2*1)+(1*8)=103
103 % 10 = 3
So 1697-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H10ClNO2/c14-10-6-2-3-7-11(10)15-13(17)9-5-1-4-8-12(9)16/h1-8,16H,(H,15,17)

1697-18-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-chlorophenyl)-2-hydroxybenzamide

1.2 Other means of identification

Product number -
Other names N-(2-Chlorophenyl)salicylamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1697-18-3 SDS

1697-18-3Relevant academic research and scientific papers

Synthesis and antiproliferative activities against Hep-G2 of salicylanide derivatives: Potent inhibitors of the epidermal growth factor receptor (EGFR) tyrosine kinase

Zhu, Zhen-Wei,Shi, Lei,Ruan, Xiao-Ming,Yang, Ying,Li, Huan-Qiu,Xu, Suo-Ping,Zhu, Hai-Liang

experimental part, p. 37 - 45 (2011/10/30)

A series of salicylanilide derivatives (compounds 1-32) were synthesised by reacting substituted salicylic acids and anilines. The chemical structures of these compounds were determined by 1H-NMR, electrospray ionisation mass spectrometry (ESI-MS) and elemental analysis. The compounds were assayed for their antiproliferative activities against the Hep-G2 cell line by the 3-(4,5-dimethylthylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method. Among the compounds tested, 22 and 28 showed the most favouable antiproliferative activities with 50% inhibitory concentration (IC50) values of 1.7 and 1.3 μM, respectively, which were comparable to the positive control of 5-fluorouracil (IC50 = 1.8 μM). A solid-phase ELISA assay was also performed to evaluate the ability of compounds 1-32 to inhibit the autophosphorylation of the epidermal growth factor receptor tyrosine kinase (EGFR TK). Docking simulations of 22 and 28 were carried out to illustrate the binding mode of the molecule into the EGFR active site, and the result suggested that both compounds 22 and 28 could bind the EGFR kinase well.

Synthesis and biological evaluation of benzamides and benzamidines as selective inhibitors of VEGFR tyrosine kinases

Nakamura, Hiroyuki,Sasaki, Yusuke,Uno, Masaharu,Yoshikawa, Tomohiro,Asano, Toru,Ban, Hyun Seung,Fukazawa, Hidesuke,Shibuya, Masabumi,Uehara, Yoshimasa

, p. 5127 - 5131 (2007/10/03)

A series of benzamidines and benzamides was synthesized as selective inhibitors of vascular endothelial growth factor receptor (VEGFR) tyrosine kinases, and tested for inhibitory activity toward autophosphorylation by the enzyme assay. Selective inhibitio

Novel Reactions: Part I - Facile Synthesis of Substituted ortho-Chloranilines from Nitrobenzene Derivatives

Ayyangar, N. R.,Kalkote, U. R.,Nikrad, P. V.

, p. 872 - 877 (2007/10/02)

N-Substituted benzo and acetohydroxamic acids (5), prepared from N-arylhydroxylamines and benzoyl or acetyl chloride, react readily with thionyl chloride at low temperature to give ortho-chloroanilide derivatives (6) in good yield.The latter (6) on hydrolysis give ortho-chloroanilines (10).Since the N-arylhydroxylamines are obtained from nitroarenes by partial reduction, the overall reaction amounts to the preparation of 10 from nitroarenes.

NOVEL ORTHOHALOGENATION REACTION. SYNTHESIS OF ORTHOCHLOROARYLAMINES FROM NITROARENES.

Ayyangar, Nagaraj R.,Kalkote, Uttam R.,Nikrad, Pandurang V.

, p. 1099 - 1102 (2007/10/02)

Thionyl chloride reacts with N-phenylbenzo and N-phenylaceto-hydroxamic acids at low temperatures to give ortho-chloroanilide derivatives in good yield.

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