76870-57-0

Basic information

• Product Name: 5-Phenyl-5,6-dihydro-benzofuro<3,2-c>chinolin-6-on
• Synonyms: 5-Phenyl-5,6-dihydro-benzofuro<3,2-c>chinolin-6-on
• CAS NO: 76870-57-0
• Molecular Weight: 311.34
• Mol File: 76870-57-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-Phenyl-5,6-dihydro-benzofuro<3,2-c>chinolin-6-on(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Phenyl-5,6-dihydro-benzofuro<3,2-c>chinolin-6-on(76870-57-0)
• EPA Substance Registry System: 5-Phenyl-5,6-dihydro-benzofuro<3,2-c>chinolin-6-on(76870-57-0)

Safety Data

• Hazardous Substances Data: 76870-57-0(Hazardous Substances Data)

Upstream product

• 76066-78-9 4-Hydroxy-1,3-diphenyl-1,2-dihydro-chinolin-2-on 
• 299215-84-2 1,2-bis(2-bromophenyl)ethanone 
• 103-72-0 phenyl isothiocyanate 
• 83-13-6 diethyl 2-phenylmalonate 
• 122-39-4 diphenylamine 
• 84261-45-0 3-Hydroxy-1,3-diphenyl-1H-quinoline-2,4-dione 
• 13683-53-9 4-Hydroxy-1,3-diphenyl-1,2,5,6,7,8-hexahydrochinolin-2-on 

Relevant articles and documents

Double heteroannulation of S,N-acetals: A facile access to quinolone derivatives

A rapid construction of quinolone fused heterocycles from single S,N-acetal precursors via double heteroannulation is described. The base, radical and metal-mediated reactions can control the C-N, C-S and C-O bond formations of the S,N-acetal with high chemoselectivity.

Synthesis of Benzofuranes by Cyclodehydrogenation of Phenylmalonyl Heterocyclic Compounds

Phenylmalonyl heterocyclic compounds such as the quinolones 1a-c or 3, benzoquinolizinones 6a, b and the phenalenones 8a, b can be converted to benzofuranes (2a-c, 7a, b and 9a, b) by cyclodehydrogenation with Pd/C in boiling diphenyl ether. 2-Phenylchinc