88474-33-3 Usage
Uses
Used in Pharmaceutical Industry:
5-CHLORO-1 H-[1,2,3]TRIAZOLE-4-CARBOXYLIC ACID METHYL ESTER is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 5-CHLORO-1 H-[1,2,3]TRIAZOLE-4-CARBOXYLIC ACID METHYL ESTER serves as a key component in the creation of agrochemicals, aiding in the production of effective pesticides and other agricultural chemicals.
Used in Materials Science:
5-CHLORO-1 H-[1,2,3]TRIAZOLE-4-CARBOXYLIC ACID METHYL ESTER is utilized as a reagent in chemical reactions, facilitating the formation of new carbon-carbon or carbon-heteroatom bonds, which are essential in advancing materials science research and applications.
Used as a Reagent in Organic Synthesis:
5-CHLORO-1 H-[1,2,3]TRIAZOLE-4-CARBOXYLIC ACID METHYL ESTER is employed as a reagent in organic synthesis, enabling the construction of complex molecular structures for a wide range of applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 88474-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,7 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88474-33:
(7*8)+(6*8)+(5*4)+(4*7)+(3*4)+(2*3)+(1*3)=173
173 % 10 = 3
So 88474-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H4ClN3O2/c1-10-4(9)2-3(5)7-8-6-2/h1H3,(H,6,7,8)
88474-33-3Relevant academic research and scientific papers
Synthesis of 4-Chloro-1,2,3-tiazole Derivatives by Diazotization of 6-Substituted 5-Amino-4-chloropyrimidines
Nemeryuk, M. P.,Sedov, A. L.,Krepelka, I.,Benes, Ya.,Safonova, T. S.
, p. 1113 - 1115 (2007/10/02)
It is shown that 4-cyano- and 4-carbalkoxy-5-chloro-1,2,3-triazoles, respectively, are formed in the diazotization of 4,6-dichloro- and 4-chloro-6-alkoxy-5-aminopyrimidines.It was observed that a methyl group in the 2 position of the starting pyrimidine derivative does not affect the structures of the reaction products under the described conditions.
