849207-19-8

Basic information

• Product Name: N-phenyl-N-(2-phenylallyl)benzamide
• Synonyms: N-phenyl-N-(2-phenylallyl)benzamide
• CAS NO: 849207-19-8
• Molecular Weight: 313.399
• Mol File: 849207-19-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-phenyl-N-(2-phenylallyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyl-N-(2-phenylallyl)benzamide(849207-19-8)
• EPA Substance Registry System: N-phenyl-N-(2-phenylallyl)benzamide(849207-19-8)

Safety Data

• Hazardous Substances Data: 849207-19-8(Hazardous Substances Data)

Upstream product

• 93-98-1 N-phenyl benzoyl amide 
• 3360-54-1 3-bromo-2-phenylprop-1-ene 
• 62-53-3 aniline 
• 98-88-4 benzoyl chloride 
• 56865-72-6 2-Phenyl-3-(phenylamino)-1-propene 

Downstream Products

• 93-98-1 N-phenyl benzoyl amide 
• 7283-47-8 (4,4-dimethylpent-1-en-2-yl)benzene 

Relevant articles and documents

Synthesis of N-Heterocycles by Dehydrogenative Annulation of N-Allyl Amides with 1,3-Dicarbonyl Compounds

Dehydrogenative annulation under oxidizing reagent-free conditions is an ideal strategy to construct cyclic structures. Reported herein is an unprecedented synthesis of pyrrolidine and tetrahydropyridine derivatives through electrochemical dehydrogenative annulation of N-allyl amides with 1,3-dicarbonyl compounds. The electrolytic method employs an organic redox catalyst, which obviates the need for oxidizing reagents and transition-metal catalysts. In these reactions, the N-allyl amides serve as a four-atom donor to react with dimethyl malonate to give pyrrolidines by a (4+1) annulation, or with β-ketoesters to afford tetrahydropyridine derivatives by a (4+2) annulation.