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Benzoic acid, 2-acetyl-3,4,5,6-tetrachloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40285-25-4

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40285-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40285-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,8 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40285-25:
(7*4)+(6*0)+(5*2)+(4*8)+(3*5)+(2*2)+(1*5)=94
94 % 10 = 4
So 40285-25-4 is a valid CAS Registry Number.

40285-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetyl-3,4,5,6-tetrachlorobenzoic acid

1.2 Other means of identification

Product number -
Other names 3',4',5',6'-Tetrachloro-2'-carboxyacetophenon

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:40285-25-4 SDS

40285-25-4Upstream product

40285-25-4Relevant academic research and scientific papers

Process for producing 2-(carboxyphenyl)-4-quinolinecarboxylic acid compounds

-

, (2008/06/13)

Quinolin-2-yl benzoic acid compounds which are useful as intermediates of quinoline compounds having angiotensin II antagonist activity prepared by decarboxylating 2-(carboxyphenyl)-4-quinolinecarboxylic acid compounds in which a carboxyl group bonded to a phenyl group may be esterified, while a carboxyl group bonded to a quinoline ring is not esterified, and both rings may have one or more substituents inert to the decarboxylation reaction.

Process for producing quinolin-2-yl benzoic acid compounds

-

, (2008/06/13)

A quinolin-2-yl benzoic acid compound useful as intermediates of angiotensin II antagonists which are effective for treating hypertension can be produced by decarboxylating a 2-carboxyphenyl-4-quinolinecarboxylic acid compound in which two carboxyl groups are not substituted and a benzene ring and a quinoline ring may have substituents inert to said decarboxylation reaction.

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