1381963-86-5

Basic information

• Product Name: 3-(1-benzenesulfonyl-4,5,6,7-tetrahydro-1H-azepin-3-yl)-acrylic acid benzyl ester
• Synonyms: 3-(1-benzenesulfonyl-4,5,6,7-tetrahydro-1H-azepin-3-yl)-acrylic acid benzyl ester
• CAS NO: 1381963-86-5
• Molecular Weight: 397.495
• Mol File: 1381963-86-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-(1-benzenesulfonyl-4,5,6,7-tetrahydro-1H-azepin-3-yl)-acrylic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-benzenesulfonyl-4,5,6,7-tetrahydro-1H-azepin-3-yl)-acrylic acid benzyl ester(1381963-86-5)
• EPA Substance Registry System: 3-(1-benzenesulfonyl-4,5,6,7-tetrahydro-1H-azepin-3-yl)-acrylic acid benzyl ester(1381963-86-5)

Safety Data

• Hazardous Substances Data: 1381963-86-5(Hazardous Substances Data)

Upstream product

• 2495-35-4 benzylacrylate 
• 4750-16-7 1-(phenylsulfonyl)-2,3,4,5-tetrahydro-1H-azepine 

Relevant articles and documents

Direct alkenylation of non-aromatic enamides via palladium-catalyzed oxidative coupling: Synthetic developments and applications

Direct C(3) alkenylation of non-aromatic enamides through palladium(II)-catalyzed Fujiwara-Moritani cross-coupling was developed. The reaction scope includes a range of cyclic enamides as well as activated alkenes. The utility of this methodology is illustrated by the synthesis of octa- or tetrahydroquinoline cores obtained from conjugated enamides via Diels-Alder cycloaddition.