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1313712-73-0

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1313712-73-0 Usage

General Description

7-Chloro-6-fluoro-2-methylquinoline-4-carboxylic acid is a chemical compound with the molecular formula C12H8ClFNO2. It is a quinoline derivative and a carboxylic acid. 7-Chloro-6-fluoro-2-Methyl-quinoline-4-carboxylic acid is used as an intermediate in the synthesis of pharmaceutical compounds and agrochemicals. It has potential biological activity and is being studied for its pharmacological properties. Its structure and properties make it a valuable building block in organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 1313712-73-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,7,1 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1313712-73:
(9*1)+(8*3)+(7*1)+(6*3)+(5*7)+(4*1)+(3*2)+(2*7)+(1*3)=120
120 % 10 = 0
So 1313712-73-0 is a valid CAS Registry Number.

1313712-73-0SDS

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 7-chloro-6-fluoro-2-methylquinoline-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 7-Chloro-6-fluoro-2-methyl-quinoline-4-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:1313712-73-0 SDS

1313712-73-0Upstream product

1313712-73-0Downstream Products

1313712-73-0Relevant articles and documents

Utilizing Solubility differences to achieve regiocontrol in the synthesis of substituted quinoline-4-carboxylic acids

Lindsay-Scott, Peter J.,Barlow, Helen

supporting information, p. 1516 - 1520 (2016/06/14)

A practical method for the regiocontrolled synthesis of substituted quinoline-4-carboxylic acids is described. Solubility differences between the product quinoline regioisomers enable their facile separation, thus avoiding any challenging chromatographic purifications and allowing access to highly substituted quinoline compounds in three steps from commercially available anilines.

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