137267-29-9 Usage
Uses
Used in Pharmaceutical Industry:
2-Isopropyl-4-methyl-1,3-thiazole-5-carboxylic acid is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure allows it to be a key component in the creation of new therapeutic agents, contributing to the development of novel treatments for a range of medical conditions.
Used in Healthcare Industry:
In the healthcare industry, 2-isopropyl-4-methyl-1,3-thiazole-5-carboxylic acid is utilized for its potential therapeutic properties. It may be incorporated into formulations that target specific health issues, leveraging its chemical characteristics to enhance the effectiveness of treatments or to introduce new modes of action against diseases.
Used in Drug Development:
2-Isopropyl-4-methyl-1,3-thiazole-5-carboxylic acid is used as a building block in drug development. Its incorporation into new chemical entities can lead to the discovery of innovative medications with improved pharmacological profiles, including better efficacy, selectivity, and safety profiles in treating various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 137267-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,6 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137267-29:
(8*1)+(7*3)+(6*7)+(5*2)+(4*6)+(3*7)+(2*2)+(1*9)=139
139 % 10 = 9
So 137267-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO2S/c1-4(2)7-9-5(3)6(12-7)8(10)11/h4H,1-3H3,(H,10,11)
137267-29-9Relevant academic research and scientific papers
Regioselectivity in the Lithiation of Methyl-substituted Thiazole- and Oxazole-Carboxylic Acids and Carboxamides: General Methods for the Elaboration of Trisubstituted Thiazoles and Oxazoles
Cornwall, Philip,Dell, Colin P.,Knight, David W.
, p. 2417 - 2428 (2007/10/02)
A number of anionic intermediates have been developed which are suitable for the elaboration of trisubstituted thiazoles and oxazoles.Thus, deprotonation of 2,4-dimethylthiazole-5-carboxylic acid 9 using either BuLi or LDA occurs regiospecifically at the
