1613511-01-5

Basic information

• Product Name: (E)-N-(3-phenylprop-1-en-1-yl)benzamide
• Synonyms: (E)-N-(3-phenylprop-1-en-1-yl)benzamide
• CAS NO: 1613511-01-5
• Molecular Weight: 237.301
• Mol File: 1613511-01-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-N-(3-phenylprop-1-en-1-yl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N-(3-phenylprop-1-en-1-yl)benzamide(1613511-01-5)
• EPA Substance Registry System: (E)-N-(3-phenylprop-1-en-1-yl)benzamide(1613511-01-5)

Safety Data

• Hazardous Substances Data: 1613511-01-5(Hazardous Substances Data)

Upstream product

• 27126-20-1 (3-azidopropyl)benzene 
• 93-97-0 benzoic acid anhydride 
• 10147-11-2 propargyl benzene 
• 61650-22-4 N-(pivaloyloxy)benzamide 
• 129423-29-6 [(1E)-3-phenylprop-1-en-1-yl]boronic acid 

Relevant articles and documents

METHOD FOR PREPARING ENAMIDE COMPOUND AND RUTHENIUM COMPLEX CATALYST USED THEREIN

Provided is a method for preparing an enamide compound, which includes reacting an organic azide compound having α-hydrogen and an anhydride by addition of a ruthenium complex catalyst in the presence of an ionic liquid, and a ruthenium complex catalyst u

Rhodium(III)-catalyzed cross-coupling of alkenylboronic acids and N -pivaloyloxylamides

Rh(III)-catalyzed umpolung amidation of alkenylboronic acids for the synthesis of enamides is reported. This reaction proceeds readily at room temperature and displays an extremely wide spectrum of functional group tolerance. With cooperation of hydrobora