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317319-34-9

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317319-34-9 Usage

General Description

2-Fluoro-4-(trifluoromethyl)thiobenzamide is a specialty chemical compound with the molecular formula C8H4F4NOS. As its name suggests, it contains elements like fluorine, carbon, hydrogen, nitrogen, oxygen, and sulfur. It is mainly used in scientific research as a reagent in the synthesis of more complex chemical substances. Detailed properties such as the melting point, boiling point, density, molar mass, and specific optical rotation, along with its accurate handling, storage, and disposal information, can be found in its Material Safety Data Sheet (MSDS). As with most chemical substances, safety precautions must be taken when handling 2-Fluoro-4-(trifluoromethyl)thiobenzamide to prevent any undesired incidents or health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 317319-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,1 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 317319-34:
(8*3)+(7*1)+(6*7)+(5*3)+(4*1)+(3*9)+(2*3)+(1*4)=129
129 % 10 = 9
So 317319-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F4NS/c9-6-3-4(8(10,11)12)1-2-5(6)7(13)14/h1-3H,(H2,13,14)

317319-34-9SDS

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-fluoro-4-(trifluoromethyl)benzenecarbothioamide

1.2 Other means of identification

Product number -
Other names 2-Fluoro-4-(trifluoromethyl)thiobenzamide

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:317319-34-9 SDS

317319-34-9Relevant articles and documents

Process development for sodelglitazar: A ppar panagonist

Brown, Andrew D.,Davis, Roman D.,Fitzgerald, Russ N.,Glover, Bobby N.,Harvey, Kim A.,Jones, Lynda A.,Liu, Bing,Patterson, Daniel E.,Sharp, Matthew J.

experimental part, p. 297 - 302 (2010/04/22)

Three efficient syntheses of sodelglitazar (1) have been developed. In particular, the third synthesis avoids the use of zinc and eliminates the resulting heavy metal waste stream as well as the potential genotoxic methanesulfonate in the two earlier syntheses. This process produces sodelglitazar in 74% overall yield from readily available thiophenol (8) and thiazole alcohol (3).

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