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35887-72-0

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35887-72-0 Usage

General Description

4-chloro-2,6-dimethylbenzoic acid is a chemical compound with the molecular formula C9H9ClO2. It is a derivative of benzoic acid, and its structure consists of a benzene ring with a carboxylic acid group and two methyl groups. The presence of a chlorine atom in the para position and the two methyl groups on the benzene ring gives this compound its specific properties. 4-chloro-2,6-dimethylbenzoic acid is used in various fields such as pharmaceuticals, agrochemicals, and as a building block in the synthesis of other chemical compounds. Its unique structure and properties make it a valuable intermediate in organic synthesis processes.

Check Digit Verification of cas no

The CAS Registry Mumber 35887-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,8 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35887-72:
(7*3)+(6*5)+(5*8)+(4*8)+(3*7)+(2*7)+(1*2)=160
160 % 10 = 0
So 35887-72-0 is a valid CAS Registry Number.

35887-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-2,6-dimethylbenzoic acid

1.2 Other means of identification

Product number -
Other names 4-chloro-2,6-dimethylbenzoic 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:35887-72-0 SDS

35887-72-0Relevant articles and documents

Preparation method for o-tolylacetic acid aryl formic acid derivative

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Paragraph 0056-0059, (2019/07/16)

The invention discloses a preparation method for an o-tolylacetic acid aryl formic acid derivative. According to the method, new C-C bonds can be formed, the organic o-tolylacetic acid aryl formic acid derivative is obtained, the good functional group tolerance is achieved, and the o-tolylacetic acid aryl formic acid derivative which cannot be easily obtained by adopting other methods can be synthesized; according to the method, adopted raw materials are easy to obtain, the yield is high, the reaction conditions are mild, the substrate range is wide, and after-treatment is simple and green.

PIPERAZINE DERIVATIVES USEFUL AS CCR5 ANTAGONISTS

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Page/Page column 31, (2010/02/12)

The use is described of CCR5 antagonists of formula (I) or a pharmaceutically acceptable salt thereof, wherein: R is optionally substituted phenyl, pyridyl, thiophenyl or naphthyl; R 1 is hydrogen or alkyl; R 2 is substituted phenyl, substituted heteroary

Carboxylic Trifluoromethanesulfonic and Methanesulfonic Anhydrides, Synthesis and Dissociation Tendency

Effenberger, Franz,Epple, Gerhard,Eberhard, Joachim K.,Buehler, Ulrich,Sohn, Erich

, p. 1183 - 1194 (2007/10/02)

Carbonyl chlorides 1 react with silver trifluoromethanesulfonate (2) and silver methanesulfonate (6) to give carboxylic trifluoromethanesulfonic anhydrides 3 and carboxylic methanesulfonic anhydrides 7, resp., in good yields; the anhydrides 3 may be synth

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