7238-62-2 Usage
General Description
ETHYL 2-CHLORO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE is a chemical compound that falls under the category of organo-sulfur compounds, specifically a thiazole. Thiazole compounds feature a five-membered ring that contains a nitrogen atom, a sulfur atom and three carbon atoms. This chemical compound, with its distinctive 2-Chloro-4-methyl-1,3-thiazole-5-carboxylic acid ethyl ester structure, is mainly known and used for its role as a chemical intermediate, playing a crucial part in several methods of organic synthesis. The exact properties of ETHYL 2-CHLORO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE, such as its melting point, boiling point, and molecular weight, may vary but are defined in accordance with standard practices in chemistry. The compound plays a key role in chemical applications and research, although data regarding its potential toxicity or environmental impact might be limited.
Check Digit Verification of cas no
The CAS Registry Mumber 7238-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,3 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7238-62:
(6*7)+(5*2)+(4*3)+(3*8)+(2*6)+(1*2)=102
102 % 10 = 2
So 7238-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H17ClN4O3/c12-6-9(17)7-15-8-13-10(16(18)19)11(15)14-4-2-1-3-5-14/h8-9,17H,1-7H2
7238-62-2Relevant articles and documents
AMINOPHENYLCYCLOPROPYL CARBOXYLIC ACIDS AND DERIVATIVES AS AGONISTS TO GPR40
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Page/Page column 67-68, (2008/06/13)
The present invention relates generally to novel therapeutic compounds and more particularly to novel compounds, their use as GPR40 agonists, processes for their manufacture, and intermediates useful in their preparation.
One pot synthesis of 1,2,4-triazoles
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, (2008/06/13)
One pot synthesis of 1,2,4-triazoles uses thioimidate intermediate and 1,2-dichloroethane solvent.
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.