160893-04-9

Basic information

• Product Name: 5-METHOXYQUINOLIN-2(1H)-ONE
• Synonyms: 5-METHOXYQUINOLIN-2(1H)-ONE
• CAS NO: 160893-04-9
• Molecular Formula: C₁₀H₉NO₂
• Molecular Weight: 175.186
• Mol File: 160893-04-9.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 5-METHOXYQUINOLIN-2(1H)-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-METHOXYQUINOLIN-2(1H)-ONE(160893-04-9)
• EPA Substance Registry System: 5-METHOXYQUINOLIN-2(1H)-ONE(160893-04-9)

Safety Data

• Hazardous Substances Data: 160893-04-9(Hazardous Substances Data)

Usage

General Description

5-METHOXYQUINOLIN-2(1H)-ONE is a chemical compound with the molecular formula C10H9NO2. It is a derivative of quinolin-2(1H)-one and contains a methoxy group attached to the 5-position of the quinoline ring. 5-METHOXYQUINOLIN-2(1H)-ONE has been studied for its potential pharmacological activities, including its antimalarial and antiproliferative properties. It has also been reported to exhibit antimicrobial and antioxidant properties. 5-METHOXYQUINOLIN-2(1H)-ONE has the potential for further development as a therapeutic agent in the pharmaceutical industry.

Upstream product

• 30557-06-3 3,4-dihydro-5-methoxy-2(1H)-quinolinone 
• 56619-93-3 N-(3-methoxyphenyl)pivalamide 
• 536-90-3 m-Anisidine 
• 82673-65-2 N-(2-formyl-3-methoxyphenyl)pivalamide 
• 578-67-6 quinolin-5-ol 
• 90924-16-6 5--methoxyquinoline N--oxide 
• 6931-19-7 5-methoxyquinoline 
• 326479-53-2 N-(3-methoxy-phenyl)-3-phenylsulfanyl-acrylamide 
• 67-56-1 methanol 
• 31570-97-5 5-hydroxyquinolin-2(1H)-one 
• 160893-07-2 2-chloro-5-methoxyquinoline 
• 186581-53-3 diazomethane 
• 611-34-7 5-Aminoquinoline 
• 607-34-1 5-nitroquinoline 

Downstream Products

• 160893-07-2 2-chloro-5-methoxyquinoline 
• 188668-90-8 5-Hydroxy-1-(p-tolyl)-1,2-dihydroquinolin-2-one 
• 188668-80-6 5-Methoxy-1-(p-tolyl)-1,2-dihydroquinolin-2-one 

Relevant articles and documents

Design, synthesis, in-vitro antiproliferative activity and kinase profile of new picolinamide based 2-amido and ureido quinoline derivatives

Abstract New 2-amido and ureido quinoline derivatives substituted with 2-N-methylamido-pyridin-4-yloxy group at the 5-position of quinoline (18 final compounds) have been designed and synthesized as anticancer sorafenib congeners. Among the synthesized de

Preparation method and application of substituted quinoline-2(1H)-one compound

The invention belongs to the field of pharmaceutical chemistry and chemical synthesis, and concretely relates to a preparation method of a substituted quinoline-2(1H)-one compound. The invention provides a preparation method of the substituted quinoline-2(1H)-one compound. The preparation method performs an oxidation reaction on a compound represented by a formula I and an oxidant in a solvent toobtain a compound represented by a formula II. The preparation method has the advantages of simple method, high yield and low cost and is suitable for industrial production. The substituted quinoline-2(1H)-one represented by the formula II is an important intermediate of a variety of pharmaceutical active ingredients.

NOVEL QUINOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS FOR PREVENTING OR TREATING CANCER CONTAINING THE SAME

The present invention refers to an excellent cancer antiproliferative potency relative to the quinoline compounds, a pharmaceutically acceptable salt, or hydrate and, number of active ingredient containing bath method and pharmaceutical composition for the prevention or treatment of cancer disease relates to search, said present invention according to compound, a pharmaceutically acceptable salt thereof, or hydrate number and number and mutant kinase protein kinase activity number of excellent cancer billion billion number activity and thus, new anticancer number is useful as the effective component can be. (by machine translation)