53551-99-8

Basic information

• Product Name: 1-BENZYL-4-METHYL-1H-QUINOLIN-2-ONE
• Synonyms: 1-BENZYL-4-METHYL-1H-QUINOLIN-2-ONE;1-BENZYL-4-METHYL-2(1H)-QUINOLINONE;1-benzyl-4-methyl-1,2-dihydroquinolin-2-one
• CAS NO: 53551-99-8
• Molecular Formula: C₁₇H₁₅NO
• Molecular Weight: 249.31
• Mol File: 53551-99-8.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-BENZYL-4-METHYL-1H-QUINOLIN-2-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BENZYL-4-METHYL-1H-QUINOLIN-2-ONE(53551-99-8)
• EPA Substance Registry System: 1-BENZYL-4-METHYL-1H-QUINOLIN-2-ONE(53551-99-8)

Safety Data

• Hazardous Substances Data: 53551-99-8(Hazardous Substances Data)

Usage

Chemical Family

1-Benzyl-4-methyl-1H-quinolin-2-one belongs to the quinolin-2-one family.

Appearance

It is a yellow powder.

Molar Mass

The molar mass is 247.29 g/mol.

Pharmacological Properties

The compound has potential pharmacological properties and is being studied for its potential use in medical and pharmaceutical research.

Anti-inflammatory Properties

1-Benzyl-4-methyl-1H-quinolin-2-one has potential anti-inflammatory properties.

Analgesic Properties

It also has potential analgesic properties.

Synthesis of Bioactive Compounds

The compound has been used in the synthesis of various bioactive compounds.

Further Research

More research is needed to fully understand its properties and potential applications.

Upstream product

• 674-82-8 4-methyleneoxetan-2-one 
• 758640-21-0 N-Benzylaniline 
• 607-66-9 4-methyl-1,2-dihydroquinolin-2-one 
• 100-39-0 benzyl bromide 
• 879682-42-5 but-3-enoic acid benzyl-(2-iodophenyl)amide 
• 615-43-0 2-iodophenylamine 
• 100-52-7 benzaldehyde 
• 76464-99-8 N-benzyl-2-iodoaniline 
• 607-66-9 4-methylquinolin-2-ol 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 490035-95-5 N-benzyl-2-(prop-1-en-2-yl)benzen-amine 
• 324738-55-8 benzyl(2-isopropenyl)carbamyl chloride 
• 201230-82-2 carbon monoxide 
• 52562-19-3 2-isopropenylaniline 

Downstream Products

• 145360-11-8 1-benzyl-4-methyl-3,4-dihydroquinolin-2(1H)-one 

Relevant articles and documents

Ru-NHC-Catalyzed Asymmetric Hydrogenation of 2-Quinolones to Chiral 3,4-Dihydro-2-Quinolones

Direct enantioselective hydrogenation of unsaturated compounds to generate chiral three-dimensional motifs is one of the most straightforward and important approaches in synthetic chemistry. We realized the Ru(II)-NHC-catalyzed asymmetric hydrogenation of 2-quinolones under mild reaction conditions. Alkyl-, aryl- and halogen-substituted optically active dihydro-2-quinolones were obtained in high yields with moderate to excellent enantioselectivities. The reaction provides an efficient and atom-economic pathway to construct simple chiral 3,4-dihydro-2-quinolones. The desired products could be further reduced to tetrahydroquinolines and octahydroquinolones.

Nucleic acid binding dyes and uses therefor

The invention provides novel compounds and compositions of Formulas I and II, as well as methods of using them. The compounds can be used, for example, to quantify an amount of double stranded DNA in a sample subjected to nucleic acid amplification, or fo

Synthesis of 2(1 H)-quinolinones via Pd-catalyzed oxidative cyclocarbonylation of 2-vinylanilines

Palladium-catalyzed oxidative cyclocarbonylation of N-monosubstituted-2- vinylanilines constitutes a simple, direct, and selective method for the synthesis of 2(1H)-quinolinones. The reaction conditions are attractive in terms of environmental considerations and operational simplicity. 2(1H)-Quinolinones with a variety of functional groups were prepared in up to 97% yield.