72850-53-4 Usage
Uses
Used in Advanced Chemistry Research:
ETHYL 2-OXO-4-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE is used as a key component in various complex reactions for advanced chemistry research. Its unique structure allows it to participate in multiple syntheses and experiments, contributing to the development of new compounds and materials.
Used in Pharmaceutical Development:
In the pharmaceutical industry, ETHYL 2-OXO-4-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE is used as an intermediate in the synthesis of potential drug candidates. Its specific chemical properties make it a valuable building block for creating new molecules with therapeutic potential.
Used in Material Science:
ETHYL 2-OXO-4-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE is employed as a precursor in the development of novel materials with unique properties. Its incorporation into these materials can lead to advancements in areas such as electronics, coatings, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 72850-53-4 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, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72850-53:
(7*7)+(6*2)+(5*8)+(4*5)+(3*0)+(2*5)+(1*3)=134
134 % 10 = 4
So 72850-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F3NO3S/c1-2-14-5(12)3-4(7(8,9)10)11-6(13)15-3/h2H2,1H3,(H,11,13)
72850-53-4Relevant articles and documents
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-Thiazolone-5-carboxylic acid ester fungicidal agents
-
, (2008/06/13)
Fungicidal compositions containing, and methods of combating fungi using, 2-thiazolone-5-carboxylic acid ester fungicidal agents of the formula SPC1 In which R1 is hydrogen; alkyl of up to 12 carbon atoms optionally substituted by phenyl, halop
