81569-27-9 Usage
Uses
Used in Pharmaceutical Industry:
4-Thiazolecarboxylicacid,2-chloro-5-(1-methylethyl)-,methylester(9CI) is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its potential therapeutic properties, including anti-inflammatory and antimicrobial effects, make it a valuable component in the development of new drugs and treatments.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Thiazolecarboxylicacid,2-chloro-5-(1-methylethyl)-,methylester(9CI) serves as an intermediate in the production of agrochemicals. Its antimicrobial properties can be harnessed to develop pesticides and other agricultural chemicals that protect crops from diseases and pests, thereby enhancing crop yield and quality.
It is crucial to handle 4-Thiazolecarboxylicacid,2-chloro-5-(1-methylethyl)-,methylester(9CI) with care due to its potential health risks if not properly managed or utilized. Proper safety measures and guidelines should be followed to ensure the safe use of this chemical in both pharmaceutical and agrochemical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 81569-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,6 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81569-27:
(7*8)+(6*1)+(5*5)+(4*6)+(3*9)+(2*2)+(1*7)=149
149 % 10 = 9
So 81569-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10ClNO2S/c1-4(2)6-5(7(11)12-3)10-8(9)13-6/h4H,1-3H3
81569-27-9Relevant academic research and scientific papers
The Preparation of Thiazole-4- and -5-carboxylates, and an Infrared Study of their Rotational Isomers
Barton, Anne,Breukelman, Stephen P.,Kaye, Perry T.,Meakins, G. Denis,Morgan, David J.
, p. 159 - 164 (2007/10/02)
Convenient general procedures have been developed for preparing series of thiazole-4- and -5-carboxylates containing alkyl and halogeno substituents.While both series of esters show i.r. carbonyl doublets caused by rotational isomerism, the more intense absorptions of the 4-carboxylates are the lower wavenumber components, whereas those of the 5-carboxylates are the higher wavenumber components.In both series the stronger bands arise from the thermochemically more stable forms; identification of these forms as the carbonyl O,S-syn-s-trans rotamers is more certain with the 4-carboxylates than with the 5-carboxylates.
