51860-35-6

Basic information

• Product Name: N-((4-methylbenzoyl)oxy)benzamide
• Synonyms: N-((4-methylbenzoyl)oxy)benzamide
• CAS NO: 51860-35-6
• Molecular Weight: 255.273
• Mol File: 51860-35-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-((4-methylbenzoyl)oxy)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-((4-methylbenzoyl)oxy)benzamide(51860-35-6)
• EPA Substance Registry System: N-((4-methylbenzoyl)oxy)benzamide(51860-35-6)

Safety Data

• Hazardous Substances Data: 51860-35-6(Hazardous Substances Data)

Upstream product

• 99-94-5 p-Toluic acid 
• 698-16-8 benzohydroximoyl chloride 
• 495-18-1 Benzohydroxamic acid 
• 874-60-2 4-methyl-benzoyl chloride 

Downstream Products

• 5079-90-3 (E)-2-styrylbenzoic acid 
• 1268451-42-8 2-((E)-4-methylstyryl)-6-((E)-styryl)benzamide 
• 1268451-11-1 (E)-N-methoxy-2-styrylbenzamide 
• 26278-74-0 3,4-dihydro-3-phenyl-1(2H)-isoquinolinone 
• 63404-82-0 (E)-2-styrylbenzamide 
• 582-78-5 N-(4-methylphenyl)benzamide 

Relevant articles and documents

Facile synthesis ofO-acylhydroxamatesviareaction of oxime chlorides with carboxylic acids

A simple and efficient method for the synthesis ofO-acylhydroxamate derivatives from oxime chlorides and carboxylic acids was developed. The reaction affords clean and facile access to diverseO-acylhydroxamates in high yields (up to 85%). The chemical structure of a typical product was confirmed using single-crystal X-ray structure analysis.

N-amidation by copper-mediated cross-coupling of organostannanes or boronic acids with O-acetyl hydroxamic acids

(Chemical Equation Presented) A general nonoxidative N-amidation of organostannanes and boronic acids has been developed. Under nonbasic conditions a wide variety of aryl, alkenyl, and heteroaryl organostannanes and boronic acids couple efficiently with O-acetyl hydroxamic acids in the presence of Cu(I) sources.