93099-45-7

Basic information

• Product Name: Benzamide, N-(5-chloro-2-hydroxyphenyl)-
• CAS NO: 93099-45-7
• Molecular Formula: C13H10ClNO2
• Molecular Weight: 247.681
• Mol File: 93099-45-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzamide, N-(5-chloro-2-hydroxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(5-chloro-2-hydroxyphenyl)-(93099-45-7)
• EPA Substance Registry System: Benzamide, N-(5-chloro-2-hydroxyphenyl)-(93099-45-7)

Safety Data

• Hazardous Substances Data: 93099-45-7(Hazardous Substances Data)

Upstream product

• 75-24-1 trimethylaluminum 
• 74993-58-1 N-(4-chlorophenoxy)benzamide 
• 197588-26-4 O-(5-Bromo-2-fluoro-phenyl)-hydroxylamine 
• 98-88-4 benzoyl chloride 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 
• 3743-70-2 N-(2-hydroxyphenyl)benzamide 
• 37593-94-5 4-chloro-2-nitrophenyl benzoate 
• 201663-88-9 N-(5-Bromo-2-fluoro-phenoxy)-benzamide 
• 36637-30-6 O-(4-chlorophenyl)hydroxylamine 
• 1027138-23-3 N-(4-Bromo-5-chloro-2-hydroxy-phenyl)-benzamide 
• 591-50-4 iodobenzene 
• 201230-82-2 carbon monoxide 
• 95-85-2 2-hydroxy-5-chloro-aniline 

Downstream Products

• 1019-90-5 5-chloro-2-phenyl-1,3-benzoxazole 

Relevant articles and documents

Iron(III) Chloride Mediated para-Selective C-H Functionalization: Access to C5-Chloro and C5,C7-Dichloro/Dianisyl Substituted 2-Arylbenzoxazoles

Iron(III) chloride mediated para-selective C?H chlorination and subsequent annulation of 2-amidophenol to synthesize C5- and C5, C7-chlorinated benzoxazoles was developed. Further, the oxidative cross-dehydrogenative coupling of amidophenol with anisole b

N-(2-hydroxyaryl)benzamide synthesis from 2-nitroaryl benzoates via an Indium-mediated reduction-migration reaction

A one-pot reduction-triggered N-(2-hydroxyaryl)benzamide synthesis from 2-nitroaryl benzoate substrates was investigated. In the presence of indium/AcOH in THF/H2O, 2-nitroaryl benzoates produced reasonable yields of the benzo group migrated N-

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.