119039-00-8

Basic information

• Product Name: N,N-dimethyl-2-((phenylsulfonyl)methyl)acrylamide
• Synonyms: N,N-dimethyl-2-((phenylsulfonyl)methyl)acrylamide
• CAS NO: 119039-00-8
• Molecular Weight: 253.322
• Mol File: 119039-00-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N,N-dimethyl-2-((phenylsulfonyl)methyl)acrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethyl-2-((phenylsulfonyl)methyl)acrylamide(119039-00-8)
• EPA Substance Registry System: N,N-dimethyl-2-((phenylsulfonyl)methyl)acrylamide(119039-00-8)

Safety Data

• Hazardous Substances Data: 119039-00-8(Hazardous Substances Data)

Upstream product

• 36526-15-5 3-(phenylsulfonyl)-2-methylenepropanoic acid 
• 506-59-2 N,N-dimethylammonium chloride 
• 89295-32-9 2-(ethoxycarbonyl)prop-2-en-1-yl phenyl sulfone 
• 2680-03-7 N,N-Dimethylacrylamide 

Downstream Products

• 119039-12-2 3-Dimethylcarbamoyl-1-methyl-cyclopent-3-enecarboxylic acid cyclohexyl ester 

Relevant articles and documents

Umpolung synthesis of branched α-functionalized amines from imines via photocatalytic three-component reductive coupling reactions

A three component reductive coupling reaction of a (hetero)aromatic amine, a (hetero)aromatic aldehyde and an electron deficient olefin catalysed by eosin Y under green LED light irradiation, for the direct generation of γ-amino acid derivatives, is described. This new umpolung synthesis of amines, which exploits the high nucleophilicity of a putative α-amino radical intermediate, generated via single electron reduction of the in situ generated imine from the Hantzsch ester terminal reductant, is efficient, operationally simple, broad in scope and offers a complementary strategy to existing synthetic approaches.