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Quinoline-4-acetic acid, with the chemical formula C10H7NO2, is a derivative of quinoline, a heterocyclic compound that features a benzene ring fused to a pyridine ring. This organic compound is recognized for its unique structure and properties, making it a valuable building block in organic synthesis and a versatile component in various applications.

109922-57-8

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109922-57-8 Usage

Uses

Used in Pharmaceutical Industry:
Quinoline-4-acetic acid is utilized as a starting material in the synthesis of a range of drugs, particularly those with anti-inflammatory and anti-tumor properties. Its role in drug development is pivotal, given its capacity to contribute to the creation of therapeutic agents that address significant health concerns.
Used in Dye and Pigment Production:
Beyond its pharmaceutical applications, quinoline-4-acetic acid also finds use in the production of dyes and pigments. Its chemical properties make it suitable for coloring applications across different industries, adding to its diverse utility.

Check Digit Verification of cas no

The CAS Registry Mumber 109922-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,2 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 109922-57:
(8*1)+(7*0)+(6*9)+(5*9)+(4*2)+(3*2)+(2*5)+(1*7)=138
138 % 10 = 8
So 109922-57-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c13-11(14)7-8-5-6-12-10-4-2-1-3-9(8)10/h1-6H,7H2,(H,13,14)

109922-57-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-quinolin-4-ylacetic acid

1.2 Other means of identification

Product number -
Other names [4]Chinolyl-essigsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:109922-57-8 SDS

109922-57-8Relevant academic research and scientific papers

STEREOSPECIFIC SYNTHESIS OF ERYTHRO CINCHONA ALKALOIDS FROM SECOLOGANIN

Brown, Richard T.,Curless, Dale

, p. 6005 - 6008 (1986)

A short, diastereoselective synthesis of (+)-dihydrocinchonine (7) and (-)-dihydrocinchonidine (8) from their biogenetic precursor, secologanin (1a), and lepidine has been achieved in 28percent overall yield.

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