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2-CHLORO-7-METHYL-QUINOLINE-3-CARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

155983-19-0

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155983-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155983-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,8 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 155983-19:
(8*1)+(7*5)+(6*5)+(5*9)+(4*8)+(3*3)+(2*1)+(1*9)=170
170 % 10 = 0
So 155983-19-0 is a valid CAS Registry Number.

155983-19-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-7-methyl-quinoline-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-CHLORO-7-METHYLQUINOLINE-3-CARBOXYLIC ACID

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:155983-19-0 SDS

155983-19-0Relevant academic research and scientific papers

Synthesis of some novel quinoline-3-carboxylic acids and pyrimidoquinoline derivatives as potential antimicrobial agents

El-Sayed, Ola A.,Al-Bassam, Badr A.,Hussein, Maher E.

, p. 403 - 410 (2002)

The synthesis and in vitro antimicrobial evaluation of several quinoline and pyrimidoquinoline derivatives are described. Treatment of 7-substituted quinolin-2(1H)-one-3-carboxylic acids 2 a-c with phosphoryl chloride or thionyl chloride gave rise to the 7-substituted 2-chloroquinoline-3-carboxylic acids 3 a-c and 7-substituted 2-chloro-3-chlorocarbonylquinolines 5 a-c respectively. The 2-chloro function in compounds 3 a-c was replaced by 2-aminothiazole or 2-aminopyridine to give 2-(thiazol-2-yl)aminoquinoline-3-carboxylic acids 4 a-c or 2-(pyrid-2-yl)aminoquinoline-3-carboxylic acids 4 d-f. Treatment of 5 a-c with the same heterocyclic amines at room temperature furnished the corresponding 7-substituted 2-chloro-3-heteryl- aminocarbonylquinolines 6a-f. The tetracyclic 9-substituted thiazolo[3′,2′: 1,2]-pyrimido[4,5-b]quinolin-5-ones 7a-c and 10-substituted pyrido[1′,2′: 1,2]- pyrimido[4,5-b]quinolin-6-ones 7 d-f were synthesized by heating 5 a-c with the heterocyclic amines in toluene or by heating 6 a-f under reflux in dimethylformamide. The products were evaluated in vitro for potential antimicrobial activity.

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