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ETHYL 2-CHLORO-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLATE is a chemical compound with the molecular formula C8H6ClF3NO2S. It is a thiazole derivative that contains an ethyl ester functional group and a chloro and trifluoromethyl substituent. ETHYL 2-CHLORO-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLATE is known for its versatile reactivity and biological activity, making it a valuable building block for the preparation of diverse chemical structures. It is also a potential candidate for further research in medicinal chemistry due to its promising biological properties.

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72850-52-3 Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 2-CHLORO-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLATE is used as an intermediate in the synthesis of various pharmaceutical drugs. Its unique chemical structure and reactivity make it a valuable component in the development of new medications with potential therapeutic benefits.
Used in Agricultural Industry:
In the agricultural sector, ETHYL 2-CHLORO-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLATE serves as an intermediate in the synthesis of agrochemicals. Its incorporation into these compounds can contribute to the development of more effective and targeted pest control solutions, enhancing crop protection and yield.
Used in Medicinal Chemistry Research:
ETHYL 2-CHLORO-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLATE is used as a building block in the preparation of diverse chemical structures for medicinal chemistry research. Its promising biological properties and versatile reactivity make it a valuable candidate for the discovery and development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 72850-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,5 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72850-52:
(7*7)+(6*2)+(5*8)+(4*5)+(3*0)+(2*5)+(1*2)=133
133 % 10 = 3
So 72850-52-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClF3NO2S/c1-2-14-5(13)3-4(7(9,10)11)12-6(8)15-3/h2H2,1H3

72850-52-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names ETHYL 2-CHLORO-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLATE

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:72850-52-3 SDS

72850-52-3Relevant articles and documents

Synthesis and Insecticidal Activity of Novel Thiazole Acrylonitrile Derivatives

Cao, Shengwen,Liu, Aiping,Liu, Weidong,Liu, Xingping,Ren, Yeguo,Pei, Hui,Huang, Lu,Zheng, Xi,Huang, Mingzhi,Wu, Daoxin

, p. 3395 - 3402 (2017/11/21)

A series of novel thiazole acrylonitrile derivatives was designed and synthesized utilizing NC-510 as a precursor. Their structures were characterized by NMR spectrometry, MS, and elemental analysis. The results of bioassay indicated that some of these ti

TETRASUBSTITUTED PYRIDAZINE HEDGEHOG PATHWAY ANTAGONISTS

-

Page/Page column 13, (2010/06/15)

The present invention provides novel tetrasubstituted pyridine hedgehog pathway antagonists of the following formula I (I) or a pharmaceutically acceptable salt thereof, wherein: X is C-R1 or N; R1 is hydrogen, fluoro or cyano; Rsup

Synthesis and biological activity of novel 2-(3-trifluoromethylphenoxy)-4-trifluoromethylthiazole-5-carboxamide derivatives

Liu, Chang-Ling,Li, Miao,Chi, Hui-Wei,Hou, Chun-Qing,Li, Zheng-Ming

, p. 796 - 799 (2008/03/27)

Novel 2-(3-trifluoromethylphenoxy)-4-trifluoromethylthiazole-5-carboxamides were designed and synthesized utilizing ethyl 3-amino-4,4,4-trifluoro-2-butenoate as a starting material via six steps. Subsequently, their biological activities were evaluated in

Syntheses and Reactions of 2-Halo-5-thiazolecarboxylates

Lee, Len F.,Schleppnik, Francis M.,Howe, Robert K.

, p. 1621 - 1630 (2007/10/02)

A variety of 2-halo-5-thiazolecarboxylates was prepared from substituted-3-aminoacrylates and 3-ketoesters.Selective reduction of 2-chloro-5-thiazolecarboxylates 4a, 4i and 4j with sodium borohydride in ethanol provided the corresponding 2-halo-5-thiazolemethanols 27 - 29.Nucleophilic displacement on methyl methanesulfonate (32c) occured selectivity at the 5-substituent to provide 2-chloro-4-(trifluoromethyl)-5-(heteroatom-substituted methyl)thiazoles 32d-f.

2,4-Disubstituted-5-thiazole-carboxylic acids and derivatives

-

, (2008/06/13)

2,4-Disubstituted-5-thiazolecarboxylic acids and derivatives thereof have been found to reduce herbicidal injury of corn, rice and sorghum plants due to the application thereto of acetamide herbicides.

2,4-Disubstituted-5-thiazole-carboxylic acids and derivatives

-

, (2008/06/13)

2,4-Disubstituted-5-thiazolecarboxylic acids and derivatives thereof have been found to reduce herbicidal injury of corn, rice and sorghum plants due to the application thereto of acetamide herbicides.

2-Chloro-4-trifluoromethyl-5-thiazolecarboxylic acids and derivatives

-

, (2008/06/13)

2-Chloro-4-trifluoromethyl-5-thiazolecarboxylic acids and derivatives thereof have been found to reduce herbicidal injury of sorghum plants due to the application thereto of 2-chloro-N-(2-methoxy-1-methylethyl)-6'-ethyl-o-acetotoluidide.

2,4-Disubstituted-5-thiazolecarboxylic acids and derivatives

-

, (2008/06/13)

2,4-Disubstituted-5-thiazolecarboxylic acids and derivatives thereof have been found to reduce herbicidal injury of corn, rice and sorghum plants due to the application thereto of acetamide herbicides.

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