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2-[2-Fluoro-4-(trifluoromethyl)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester is a complex organic compound featuring a thiazole ring and a trifluoromethylphenyl group. It is an ethyl ester derivative of thiazolecarboxylic acid, known for its versatile reactivity and the potential to introduce fluorine atoms into target molecules. The presence of both fluorine and methyl groups in its structure, along with the unique pharmacological properties of the thiazole ring, makes it a valuable component in drug discovery and development, as well as in the synthesis of pharmaceuticals and agrochemicals.

317319-35-0

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317319-35-0 Usage

Uses

Used in Pharmaceutical Synthesis:
2-[2-Fluoro-4-(trifluoromethyl)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester is used as a building block in the pharmaceutical industry for the synthesis of various drugs. Its unique molecular structure, including the thiazole ring and trifluoromethylphenyl group, allows for the development of new therapeutic agents with improved pharmacological properties.
Used in Agrochemical Development:
In the agrochemical industry, 2-[2-Fluoro-4-(trifluoromethyl)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester is utilized as a key intermediate in the synthesis of agrochemicals. Its reactivity and the ability to introduce fluorine atoms into target molecules contribute to the creation of more effective and environmentally friendly pesticides and other agricultural chemicals.
Used in Drug Discovery:
2-[2-Fluoro-4-(trifluoromethyl)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester is employed as a starting material in drug discovery for its potential to introduce unique pharmacological properties. The presence of the thiazole ring and the ability to modify the molecule through the introduction of fluorine and methyl groups make it an important target for the development of novel therapeutic agents with enhanced efficacy and selectivity.
Used in Fluorine Chemistry:
2-[2-Fluoro-4-(trifluoromethyl)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester is used as a reagent in fluorine chemistry for the synthesis of fluorinated compounds. The presence of fluorine atoms in its structure allows for the exploration of the unique chemical and biological properties of fluorinated molecules, which can lead to the development of new materials and pharmaceuticals with improved performance.

Check Digit Verification of cas no

The CAS Registry Mumber 317319-35-0 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 317319-35:
(8*3)+(7*1)+(6*7)+(5*3)+(4*1)+(3*9)+(2*3)+(1*5)=130
130 % 10 = 0
So 317319-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H11F4NO2S/c1-3-21-13(20)11-7(2)19-12(22-11)9-5-4-8(6-10(9)15)14(16,17)18/h4-6H,3H2,1-2H3

317319-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names 2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester

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:317319-35-0 SDS

317319-35-0Relevant academic research and scientific papers

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).

PROCESS FOR PREPARATION OF CHEMICAL COMPOUNDS

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Page/Page column 34-35, (2010/02/07)

The present invention relates to a process for the preparation of certain chemical compounds. In particular, the present invention relates to a method for the preparation of compounds that have been shown to activate human peroxisome proliferator activate

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