97305-91-4

Basic information

• Product Name: (Z)-N-benzyl-N-(1-methyl-2-phenylvinyl)acetamide
• Synonyms: (Z)-N-benzyl-N-(1-methyl-2-phenylvinyl)acetamide
• CAS NO: 97305-91-4
• Molecular Weight: 265.355
• Mol File: 97305-91-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (Z)-N-benzyl-N-(1-methyl-2-phenylvinyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-N-benzyl-N-(1-methyl-2-phenylvinyl)acetamide(97305-91-4)
• EPA Substance Registry System: (Z)-N-benzyl-N-(1-methyl-2-phenylvinyl)acetamide(97305-91-4)

Safety Data

• Hazardous Substances Data: 97305-91-4(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 108-86-1 bromobenzene 
• 1042139-23-0 N-benzyl-N-(prop-1-en-2-yl)acetamide 
• 780-69-8 triethoxyphenylsilane 
• 18793-46-9 (E)-N-(1-Methyl-2-phenylethenyl)ethanamide 
• 100-44-7 benzyl chloride 
• 18793-46-9 (Z)-N-(1-Methyl-2phenylethenyl)ethanamide 

Downstream Products

• 14593-16-9 N-acetylamphetamine 
• 100835-72-1 N-benzyl-N-(1-methyl-2-phenylethyl)acetamide 
• 588-46-5 N-(phenylmethyl)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.