1392296-72-8

Basic information

• Product Name: N-benzyl-N-(1-(p-tolyl)vinyl)acetamide
• Synonyms: N-benzyl-N-(1-(p-tolyl)vinyl)acetamide
• CAS NO: 1392296-72-8
• Molecular Weight: 265.355
• Mol File: 1392296-72-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-benzyl-N-(1-(p-tolyl)vinyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-N-(1-(p-tolyl)vinyl)acetamide(1392296-72-8)
• EPA Substance Registry System: N-benzyl-N-(1-(p-tolyl)vinyl)acetamide(1392296-72-8)

Safety Data

• Hazardous Substances Data: 1392296-72-8(Hazardous Substances Data)

Upstream product

• 2089-33-0 4-methylacethophenone oxime 
• 100-39-0 benzyl bromide 
• 177750-08-2 1-(4-methylphenyl)ethenylacetamide 
• 122-00-9 para-methylacetophenone 

Downstream Products

• 1392296-97-7 (Z)-N-benzyl-N-(2-phenyl-1-(p-tolyl)vinyl)acetamide 
• 6097-27-4 2-thiocyanato-1-(4-tolyl)ethanone 
• 58-72-0 Triphenylethylene 
• 26189-62-8 phenyl 2,2-diphenylethenyl sulfone 
• 1392297-86-7 (E)-N-benzyl-N-(1,2-diphenylvinyl)acetamide 

Relevant articles and documents

Rhodium(III)-Catalyzed Direct C-H Arylation of Various Acyclic Enamides with Arylsilanes

The stereoselective β-C(sp2)-H arylation of various acyclic enamides with arylsilanes via Rh(III)-catalyzed cross-coupling reaction was illustrated. The methodology was characterized by extraordinary efficacy and stereoselectivity, a wide scope of substrates, good functional group tolerance, and the adoption of environmentally friendly arylsilanes. The utility of this present method was evidenced by the gram-scale synthesis and further elaboration of the product. In addition, Rh(III)-catalyzed C-H activation is considered to be the critical step in the reaction mechanism.