1369531-69-0

Basic information

• Product Name: (S)-benzyl 4-oxo-2-phenyl-3,4-dihydroquinoline-1(2H)-carboxylate
• CAS NO: 1369531-69-0
• Molecular Weight: 357.409
• Mol File: 1369531-69-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-benzyl 4-oxo-2-phenyl-3,4-dihydroquinoline-1(2H)-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-benzyl 4-oxo-2-phenyl-3,4-dihydroquinoline-1(2H)-carboxylate(1369531-69-0)
• EPA Substance Registry System: (S)-benzyl 4-oxo-2-phenyl-3,4-dihydroquinoline-1(2H)-carboxylate(1369531-69-0)

Safety Data

• Hazardous Substances Data: 1369531-69-0(Hazardous Substances Data)

Upstream product

• 172538-83-9 benzyl 4-oxoquinoline-1(4H)-carboxylate 
• 98-80-6 phenylboronic acid 

Relevant articles and documents

Palladium-catalyzed asymmetric conjugate addition of arylboronic acids to heterocyclic acceptors

Flava Flavanone: Asymmetric conjugate additions to chromones and 4-quinolones are reported utilizing a single catalyst system formed in situ from Pd(OCOCF3)2 and (S)-tBuPyOX. Notably, these reactions are performed in wet solvent under ambient atmosphere, and employ readily available arylboronic acids as the nucleophile, thus providing ready access to these asymmetric heterocycles (see scheme).