32262-18-3

Basic information

• Product Name: 4-METHOXY-1-METHYL-2(1H)-QUINOLINONE
• Synonyms: 4-METHOXY-1-METHYL-2(1H)-QUINOLINONE;4-Methoxy-N-Methyl-2-quinolone;N-Methyl-4-methoxycarbostyril;4-Methoxy-1-Methylquinolin-2-one
• CAS NO: 32262-18-3
• Molecular Formula: C₁₁H₁₁NO₂
• Molecular Weight: 189
• Mol File: 32262-18-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 303.7oC at 760 mmHg
• Flash Point: 137.5°C
• Appearance: /
• Density: 1.21g/cm3
• Vapor Pressure: 0.000913mmHg at 25°C
• Refractive Index: 1.597
• CAS DataBase Reference: 4-METHOXY-1-METHYL-2(1H)-QUINOLINONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXY-1-METHYL-2(1H)-QUINOLINONE(32262-18-3)
• EPA Substance Registry System: 4-METHOXY-1-METHYL-2(1H)-QUINOLINONE(32262-18-3)

Safety Data

• Hazardous Substances Data: 32262-18-3(Hazardous Substances Data)

Usage

General Description

4-METHOXY-1-METHYL-2(1H)-QUINOLINONE is a chemical compound with the molecular formula C11H11NO2. It is a quinolone derivative with a methoxy group at the 4-position and a methyl group at the 1-position. 4-METHOXY-1-METHYL-2(1H)-QUINOLINONE has been studied for its potential pharmaceutical properties, including its use as an antimalarial agent and its ability to inhibit the growth of cancer cells. It has also been investigated for its potential use in organic synthesis and as a building block for creating new pharmaceutical compounds. As a quinolone derivative, 4-METHOXY-1-METHYL-2(1H)-QUINOLINONE has the potential to be used in a variety of applications within the pharmaceutical and chemical industries.

InChI:InChI=1/C11H11NO2/c1-12-9-6-4-3-5-8(9)10(14-2)7-11(12)13/h3-7H,1-2H3

Upstream product

• 186581-53-3 diazomethane 
• 70254-44-3 2,4-dihydroxyquinoline 
• 61469-95-2 1-methyl-1H-quinoline-2,4-dione 
• 77-78-1 dimethyl sulfate 
• 27667-34-1 4-methoxy-2-hydroxyquinoline 
• 74-88-4 methyl iodide 
• 1677-46-9 4-hydroxy-1-methyl-2(1H)-quinolone 
• 70254-43-2 4-Hydroxy-2-quinolone 
• 27667-34-1 4-methoxyquinolin-2(1H)-one 
• 124-41-4 sodium methylate 
• 39581-30-1 3-(N-methyl-N-phenylamino)-3-oxopropanenitrile 
• 60657-74-1 3-(methyl(phenyl)amino)-3-oxopropanoic acid 
• 42014-51-7 bromoacetic acid N-hydroxusuccinimidyl ester 
• 85-91-6 Methyl N-methylanthranilate 

Downstream Products

• 61469-95-2 1-methyl-1H-quinoline-2,4-dione 
• 13849-56-4 Edulinin 

Relevant articles and documents

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Synthesis of 3,4-disubstituted quinolin-2-(1H)-ones via palladium-catalyzed decarboxylative arylation reactions

The Pd-catalyzed decarboxylative cross-coupling reaction of 4-substituted quinolin-2(1H)-one-3-carboxylic acids with (hetero)aryl halides is described. With palladium(II) bromide and triphenylarsine ligand as the catalyst system, a variety of 4-substituted 3-(hetero)aryl quinolin-2(1 H)-ones and related heterocycles, such as 4-substituted 3-arylcoumarins can be prepared in good to excellent yields. Copyright

BACTERIOSTATIC HETEROCYCLES FROM EUODIA LUNU-ANKENDA

A new constituent characterized as 8-acetyl-3,4-dihydroxy-5,7-dimethoxy-2,2-dimethylchroman has been isolated together with alloevodionol-7-methyl ether, 4-methoxy-1-methyl-2(1H) quinolinone, evolitrine, isoevodionol and its methyl ether from the aerial parts of Euodia lunu-ankenda.Its structure was confirmed by its transformation to alloevodionol-7-methyl ether. 4-Methoxy-1-methyl-2(1H)quinolinone and its isomer were synthesized by a modified procedure.Key Word Index - Euodia lunu-ankenda; Rutaceae; 8-acetyl-3,4-dihydroxy-5,7-dimethoxy-2,2-dimethylchroman; alloevodionol-7-methyl ether; 4-methoxy-1-methyl-2(1H)quinolinone; isoevodionol; isoevodionol methyl ether; antibacterial activity.