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159870-86-7

159870-86-7

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159870-86-7 Usage

Chemical Properties

White solid

Uses

2-Chloro-6-trifluoromethylbenzothiazole

Check Digit Verification of cas no

The CAS Registry Mumber 159870-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,8,7 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 159870-86:
(8*1)+(7*5)+(6*9)+(5*8)+(4*7)+(3*0)+(2*8)+(1*6)=187
187 % 10 = 7
So 159870-86-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H3ClF3NS/c9-7-13-5-2-1-4(8(10,11)12)3-6(5)14-7/h1-3H

159870-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-6-trifluoromethylbenzothiazole

1.2 Other means of identification

Product number -
Other names 2-chloro-6-(trifluoromethyl)-1,3-benzothiazole

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:159870-86-7 SDS

159870-86-7Downstream Products

159870-86-7Relevant articles and documents

DERIVATIVES OF 2 -AMINTHIAZOLES AND 2-AMINOOXAZOLES, PROCESSES FOR THEIR PREPARATION AND THEIR USE AS PHARMACEUTICALS

-

Page/Page column 67-68, (2010/11/26)

The invention relates to derivatives of 2-aminothiazoles and 2-aminooxazoles in all its stereoisomeric forms, enantiomeric forms and mixtures in any ratio, and its physiologically acceptable salts and tautomeric forms showing PPARdelta agonist activity. W

A convenient synthesis of 2-mercapto and 2-chlorobenzothiazoles

Zhu, Lei,Zhang, Mingbao,Dai, Miao

, p. 727 - 730 (2007/10/03)

A convenient synthesis of 2-mercapto and 2-chlorobenzothiazoles is described. The key feature of the synthesis is an exclusive ortho-selective nucleophilic aromatic substitution reaction of ortho-haloanilines with potassium/sodium O-ethyl dithiocarbonate under mild conditions. Subsequent intra-molecular cyclization affords 2-mercaptobenzothiazoles in high yields. The 2-mercaptobenzothiazoles are readily converted to corresponding 2-chlorobenzothiazoles upon treatment with sulfuryl chloride.

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