96600-76-9

Basic information

• Product Name: 4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone
• Synonyms: 4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone;4-Chloro-1-Methyl-2-oxo-1,2-dihydroquinoline-3-carbaldehyde
• CAS NO: 96600-76-9
• Molecular Formula: C₁₁H₈ClNO₂
• Molecular Weight: 221.63972
• Mol File: 96600-76-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone(96600-76-9)
• EPA Substance Registry System: 4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone(96600-76-9)

Safety Data

• Hazardous Substances Data: 96600-76-9(Hazardous Substances Data)

Usage

General Description

4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone, also known as 4-Chloro-3-formyl-1-methylquinolin-2(1H)-one, is a chemical compound with the molecular formula C11H9NO2Cl. It is a quinolinone derivative that contains a chlorine atom, a formyl group, and a methyl group attached to the quinoline ring. 4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone has potential pharmacological properties and may be used as a building block in the synthesis of pharmaceutical drugs. It is also known for its role as an intermediate in the preparation of various pharmaceutical and fine chemical products. Additionally, it may exhibit certain biological activities and has potential applications in the field of medicinal chemistry and drug discovery.

Upstream product

• 132911-20-7 3-<(2,6-dimethylphenyl)aminomethylene>-1-methyl-2,4(1H,3H)-quinolinedione 
• 65740-49-0 1-methyl-3-formyl-4-hydroxy-2(1H)-quinolinone 
• 1677-46-9 4-hydroxy-1-methyl-2(1H)-quinolone 
• 68-12-2 N,N-dimethyl-formamide 
• 59856-28-9 1-methyl-3-(phenylaminomethylene)-2,4-(1H,3H)-quinolinedione 
• 132911-16-1 4-chloro-3-(dichloromethyl)-1-methyl-2(1H)-quinolone 

Relevant articles and documents

Nucleophilic Chlorination of 3-Formyl-4-hydroxy-quinolin-2(1H)-ones

Chlorination of 1-substituted 3-formyl-4-hydroxy-2-quinolones (1a, b) with phosphorylchloride leads to 4-chloro-3-dichloromethylquinolones (2), which can be hydrolyzed to 4-chloro-3-formylquinolones (4).From the anilinomethylene quinolinediones (3), at lo

Chemistry of Carbostyril: Part I - Oxidation Reactions of 4-Hydroxy- and 4-Hydroxy-1-methyl-2(1H)-quinolinones

4-Hydroxy-2(1H)-quinolinone (1) reacts with acetic anhydride in dimethylsulphoxide at 100 deg to afford 3-dimethylsulfonioquinoline-2,4-dionate (3) whereas 3,3'-methylenebis (4) and 2,3,4,5,1',2',3',4'-octahydro-4,2',4'-trioxospioroquinoline-2,3'-quinoline> (5) are formed when the reaction is carried out at 165-70 deg.The involvement of 4 as a precursor of 5 has been demonstrated.Probable mechanisms of their formation have been proposed.The behaviour of 4-hydroxy-1-methyl-2(1H)-quinolinone (2) towards other oxidising agents, such as HNO3, CrO3, SOCl2-DMF and p-benzoquinone has also been studied.