3743-12-2

Basic information

• Product Name: N-(4-chloro-2-hydroxyphenyl)benzamide
• Synonyms: N-(4-chloro-2-hydroxyphenyl)benzamide
• CAS NO: 3743-12-2
• Molecular Weight: 247.681
• Mol File: 3743-12-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-(4-chloro-2-hydroxyphenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-chloro-2-hydroxyphenyl)benzamide(3743-12-2)
• EPA Substance Registry System: N-(4-chloro-2-hydroxyphenyl)benzamide(3743-12-2)

Safety Data

• Hazardous Substances Data: 3743-12-2(Hazardous Substances Data)

Upstream product

• 2866-82-2 N-(4-chlorophenyl)benzamide 
• 28443-50-7 2-amino-5-chlorophenol 
• 93-97-0 benzoic acid anhydride 
• 98-88-4 benzoyl chloride 
• 74993-54-7 O-(m-chloro-phenyl)-hydroxylamine 
• 74993-59-2 N-(3-Chloro-phenoxy)-benzamide 
• 92044-52-5 1-(benzyloxy)-4-chloro-2-nitrobenzene 

Downstream Products

• 15952-20-2 6-chloro-2-phenylbenzo[d]oxazole 
• 877858-36-1 (8-chloro-3,4-dihydrobenzo[b][1,4]oxazepin-5(2H)-yl)(phenyl)methanone 

Relevant articles and documents

PYRAZOLO[1,5a]PYRIMIDINE DERIVATIVES AS IRAK4 MODULATORS

Compounds of Formula (0), Formula (I), and Formula (II) and methods of use as Interleukin-1 Receptor Associated Kinase (IRAK4) inhibitors are described herein.

Anacardic acid derived salicylates are inhibitors or activators of lipoxygenases

Lipoxygenases catalyze the oxidation of unsaturated fatty acids, such as linoleic acid, which play a crucial role in inflammatory responses. Selective inhibitors may provide a new therapeutic approach for inflammatory diseases. In this study, we describe

AlCl3-mediated migration of benzamido group of N-phenoxybenzamide derivatives to the phenyl group

AlCl3-mediated decomposition of N-phenoxybenzamide derivatives in dichloromethane mainly leads to regioselective intramolecular migration of benzamido group from the oxygen to the ortho position of the phenyl group via electron-deficient nitrogen intermediates.