70216-33-0

Basic information

• Product Name: N-(2-(3,4-dimethoxyphenyl)-2-oxoethyl)benzamide
• Synonyms: N-(2-(3,4-dimethoxyphenyl)-2-oxoethyl)benzamide
• CAS NO: 70216-33-0
• Molecular Weight: 299.326
• Mol File: 70216-33-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(2-(3,4-dimethoxyphenyl)-2-oxoethyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-(3,4-dimethoxyphenyl)-2-oxoethyl)benzamide(70216-33-0)
• EPA Substance Registry System: N-(2-(3,4-dimethoxyphenyl)-2-oxoethyl)benzamide(70216-33-0)

Safety Data

• Hazardous Substances Data: 70216-33-0(Hazardous Substances Data)

Upstream product

• 187101-52-6 2-azido-1-(3,4-dimethoxyphenyl)ethanone 
• 65-85-0 benzoic acid 
• 98-88-4 benzoyl chloride 
• 91-16-7 1,2-dimethoxybenzene 
• 53587-10-3 hippuryl chloride 

Downstream Products

• 499-61-6 arterenone 
• 70216-32-9 5-(3,4-dimethoxyphenyl)-2-phenyl-1,3-oxazole 
• 71527-21-4 N-[2-(3,4-dimethoxy-phenyl)-[1,3]dioxolan-2-ylmethyl]-benzamide 
• 111638-16-5 6',7'-dimethoxy-1'-phenyl-3'H-spiro[[1,3]dioxolane-2,4'-isoquinoline] 

Relevant articles and documents

Synthesis of α-Amidoketones through the Cascade Reaction of Carboxylic Acids with Vinyl Azides under Catalyst-Free Conditions

An efficient synthesis of α-amidoketone derivatives through the cascade reactions of carboxylic acids with vinyl azides is presented. Compared with literature protocols, notable features of this new method include catalyst-free conditions, broad substrate scope, good tolerance of a wide range of functional groups, and high efficiency. In addition, the synthetic potential of this method as a tool for late-stage modification was convincingly manifested by its application in the structural elaborations of a number of carboxylic acid drug molecules.