72850-61-4 Usage
Description
2-CHLORO-4-(TRIFLUOROMETHYL)THIAZOLE-5-CARBOXYLIC ACID is a chlorinated thiazole derivative with the molecular formula C6H3ClF3NO2S. It features a trifluoromethyl group and a carboxylic acid functional group, making it a versatile compound with potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
2-CHLORO-4-(TRIFLUOROMETHYL)THIAZOLE-5-CARBOXYLIC ACID is used as a building block for the synthesis of biologically active compounds. Its unique structure and functional groups contribute to the development of novel drug candidates, enhancing the therapeutic potential of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-CHLORO-4-(TRIFLUOROMETHYL)THIAZOLE-5-CARBOXYLIC ACID serves as an intermediate for the production of crop-protection agents. Its properties allow for the creation of innovative compounds that can protect crops from pests and diseases, thereby increasing agricultural productivity.
Used as a Research Tool in Chemical Biology:
2-CHLORO-4-(TRIFLUOROMETHYL)THIAZOLE-5-CARBOXYLIC ACID is utilized as a research tool in chemical biology, where its unique structure aids in understanding complex biological processes and interactions at the molecular level.
Used as a Research Tool in Medicinal Chemistry:
Similarly, in medicinal chemistry, this compound is employed as a research tool to explore its potential in the development of new therapeutic agents, taking advantage of its chemical properties to probe and modulate biological targets.
Check Digit Verification of cas no
The CAS Registry Mumber 72850-61-4 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, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72850-61:
(7*7)+(6*2)+(5*8)+(4*5)+(3*0)+(2*6)+(1*1)=134
134 % 10 = 4
So 72850-61-4 is a valid CAS Registry Number.
72850-61-4Relevant 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
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.
