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37526-67-3

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37526-67-3 Usage

General Description

2-(Trifluoromethylthio)benzoic acid is a chemical compound with the molecular formula C8H5F3O2S. It is a derivative of benzoic acid, featuring a trifluoromethylthio group attached to the benzene ring. 2-(TRIFLUOROMETHYLTHIO)BENZOIC ACI is an organothio compound, which contains a sulfur atom bonded to a benzene ring. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in research laboratories for various chemical reactions. 2-(TRIFLUOROMETHYLTHIO)BENZOIC ACI is known for its strong inhibitory effects on the growth of certain pests and parasites, making it a valuable component in the production of insecticides and other agricultural products.

Check Digit Verification of cas no

The CAS Registry Mumber 37526-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,2 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37526-67:
(7*3)+(6*7)+(5*5)+(4*2)+(3*6)+(2*6)+(1*7)=133
133 % 10 = 3
So 37526-67-3 is a valid CAS Registry Number.

37526-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(trifluoromethylsulfanyl)benzoic acid

1.2 Other means of identification

Product number -
Other names 2-((Trifluoromethyl)thio)benzoic 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:37526-67-3 SDS

37526-67-3Relevant articles and documents

Trifluoromethylation of thiophenols and thiols with sodium trifluoromethanesulfinate and iodine pentoxide

Ma, Jing-Jing,Yi, Wen-Bin,Lu, Guo-Ping,Cai, Chun

, p. 417 - 421 (2016/02/03)

A selective and facile trifluoromethylation process for a wide range of thiophenols and thiols under metal free conditions has been developed using two simple and safe solids, sodium trifluoro-methanesulfinate and iodine pentoxide, via the radical process.

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