132089-40-8 Usage
Uses
Used in Pharmaceutical Industry:
4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester is used as a chemical intermediate for the synthesis of pharmaceuticals. It serves as a key component in the creation of new drugs, contributing to the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester is utilized as an intermediate in the production of agrochemicals. Its role in this industry is pivotal for the synthesis of compounds that can enhance crop protection and management.
Safety Precautions:
It is crucial to handle 4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester with care and adhere to proper safety measures. 4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester may present health and environmental risks if not used and disposed of correctly, necessitating responsible practices in its application and management.
Check Digit Verification of cas no
The CAS Registry Mumber 132089-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,8 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132089-40:
(8*1)+(7*3)+(6*2)+(5*0)+(4*8)+(3*9)+(2*4)+(1*0)=108
108 % 10 = 8
So 132089-40-8 is a valid CAS Registry Number.
132089-40-8Relevant academic research and scientific papers
N-H Insertion reactions of rhodium carbenoids. Part 5: A convenient route to 1,3-azoles
Davies, James R.,Kane, Peter D.,Moody, Christopher J.
, p. 3967 - 3977 (2007/10/03)
Dirhodium(II) carboxylate catalysed reaction of diazocarbonyl compounds 2 in the presence of primary amides 1 results in the formation of α-acylaminoketones 3 (12 examples) by N-H insertion reaction of the intermediate rhodium carbene. The 1,4-dicarbonyl
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
