56969-73-4

Basic information

• Product Name: (4-methylquinolin-3-yl)(phenyl)methanone
• Synonyms: (4-methylquinolin-3-yl)(phenyl)methanone
• CAS NO: 56969-73-4
• Molecular Weight: 247.296
• Mol File: 56969-73-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (4-methylquinolin-3-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-methylquinolin-3-yl)(phenyl)methanone(56969-73-4)
• EPA Substance Registry System: (4-methylquinolin-3-yl)(phenyl)methanone(56969-73-4)

Safety Data

• Hazardous Substances Data: 56969-73-4(Hazardous Substances Data)

Upstream product

• 1859-70-7 N-(2-acetylphenyl)-4-methylbenzenesulfonamide 
• 3623-15-2 phenyl propargyl ketone 
• 551-93-9 2-aminoacetophenone 
• 93-55-0 1-phenyl-propan-1-one 
• 4127-53-1 3-methylbenzo[c]isoxazole 
• 1201-93-0 1-phenyl-3-dimethylaminoprop-2-enone 
• 1794-48-5 1-bromo-3-phenylprop-2-yne 
• 1571120-17-6 (4-methyl-1-tosyl-1,2-dihydroquinolin-3-yl)(phenyl)methanone 
• 1571120-88-1 N-(2-acetylphenyl)-4-methyl-N-(3-phenylprop-2-ynyl)benzenesulfonamide 
• 941706-81-6 1-(2-aminophenyl)ethanol 

Relevant articles and documents

Chemoselective Synthesis of N -Arylenaminones and 3-Aroylquinolines by Synergistic Control of Temperature and Amount of Catalyst

An efficient and practical method has been developed for the divergent synthesis of N -arylenaminones and 3-aroylquinolines from 2-aminoaryl ketones and N, N -dimethylenaminones in the presence of 4-toluenesulfonic acid through synergistic control of the

ZnCl2-promoted Friedl?nder-type synthesis of 4-substituted 3-aroyl quinolines from o-aminoaryl ketones and enaminones

A practical synthesis of 4-substituted 3-aroyl quinolines via Friedl?nder-type reaction from readily available o-aminoaryl ketones and enaminones was developed. In the presence of ZnCl2, the reaction proceeded smoothly affording the desired products with various functional groups in moderate to good yields.