312514-88-8

Basic information

• Product Name: N-(3-acetamidophenyl)benzamide
• Synonyms: N-(3-acetamidophenyl)benzamide
• CAS NO: 312514-88-8
• Molecular Weight: 254.288
• Mol File: 312514-88-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(3-acetamidophenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-acetamidophenyl)benzamide(312514-88-8)
• EPA Substance Registry System: N-(3-acetamidophenyl)benzamide(312514-88-8)

Safety Data

• Hazardous Substances Data: 312514-88-8(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 16091-26-2 N-Benzoyl-m-phenylendiamin 

Downstream Products

• 1152493-94-1 N-(2-phenylbenzoxazol-7-yl)acetamide 
• 1152493-96-3 N-(2-methylbenzoxazol-7-yl)benzamide 

Relevant articles and documents

Copper-catalyzed synthesis of benzoxazoles via a regioselective C-H functionalization/C-O bond formation under an air atmosphere

(Chemical Equation Presented) An efficient method for the synthesis of functionalized benzoxazoles is described that involves a copper(II)-catalyzed regioselective C-H functionalization/C-O bond formation protocol. The use of dichlorobenzene as a solvent at 160°C allows the use of air as the terminal oxidant in the catalytic synthesis of benzoxazoles in a process that has high functional group tolerance. The presence of a directing group at the meta position markedly improves the reaction efficacy and a variety of 7-substituted benzoxazoles are selectively produced under mild reaction conditions. The mechanism of the reaction is also discussed in this report.