1197391-19-7

Basic information

• Product Name: 4-bromo-2-phenylquinolin-3-ol
• Synonyms: 4-bromo-2-phenylquinolin-3-ol
• CAS NO: 1197391-19-7
• Molecular Weight: 300.154
• Mol File: 1197391-19-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-bromo-2-phenylquinolin-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-bromo-2-phenylquinolin-3-ol(1197391-19-7)
• EPA Substance Registry System: 4-bromo-2-phenylquinolin-3-ol(1197391-19-7)

Safety Data

• Hazardous Substances Data: 1197391-19-7(Hazardous Substances Data)

Upstream product

• 7152-68-3 2,3-epoxy-1-phenyl-3-(2-nitrophenyl)-1-propanone 
• 485-89-2 oxycinchophen 
• 71-43-2 benzene 
• 532-27-4 1-chloroacetophenone 
• 552-89-6 2-nitro-benzaldehyde 
• 7152-68-3 trans-2,3-epoxy-1-(2-nitrophenyl)-3-phenylpropan-1-one 
• 5855-50-5 3-hydroxy-2-phenylquinoline 

Downstream Products

• 31588-18-8 3-hydroxy-2-phenyl-1H-quinolin-4-one 

Relevant articles and documents

[2-(2-Nitrophenyl)oxiran-1-yl](aryl(methyl))ketones in the synthesis of 3-hydroxyquinolin-4(1H)-ones and 2-arylquinolines

The applicability of [2-(2-nitrophenyl)oxiran-1-yl](aryl(methyl))ketones in the synthesis of 3-hydroxyquinolin-4-ones and 2-arylquinolines was studied.

Bromodecarboxylation of quinoline salicylic acids: Increasing the diversity of accessible substituted quinolines

(Chemical Equation Presented) Quinoline salicylic acids underwent bromodecarboxylation at room temperature upon treatment with N-bromosuccinimide. A wide variety of functional groups was tolerated. Several one-pot transformations were also carried out, allowing the preparation of diverse 4-substituted quinolines.