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[1,2,4]Triazole-1-carboxylic acid 2,2,2-trichloro-ethyl ester is a chemical compound with the molecular formula C6H6Cl3N3O2. It is an ester derivative of [1,2,4]triazole-1-carboxylic acid, featuring a 2,2,2-trichloroethyl group attached to the carboxylic acid moiety. [1,2,4]Triazole-1-carboxylic acid 2,2,2-trichloro-ethyl ester is known for its potential applications in various chemical and pharmaceutical processes, such as the synthesis of agrochemicals and pharmaceuticals. It is characterized by its stability and reactivity, which can be exploited in the formation of various chemical bonds. The compound's structure and properties make it a valuable intermediate in the development of new compounds with specific therapeutic or pesticidal properties.

90160-96-6

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90160-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90160-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,6 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90160-96:
(7*9)+(6*0)+(5*1)+(4*6)+(3*0)+(2*9)+(1*6)=116
116 % 10 = 6
So 90160-96-6 is a valid CAS Registry Number.

90160-96-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-1,2,4-Triazole-1-carboxylic acid, 2,2,2-trichloroethyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:90160-96-6 SDS

90160-96-6Relevant academic research and scientific papers

A NEW OXIGENATING METHOD USING 1-ALKOXYCARBONYL-1,2,4-TRIAZOLES AND HYDROGEN PEROXIDE RELATIVE REACTIVITY OF O-ALKYLPEROXYCARBONIC ACIDS

Tsunokawa, Youko,Iwasaki, Shigeo,Okuda, Shigenobu

, p. 4578 - 4581 (2007/10/02)

A convenient method is reported for the epoxidation of alkenes and the Baeyer-Villiger oxidation of a variety of carbonyl compounds using the 1-alkoxycarbonyl-1,2,4-triazoles (1a-c)/H2O2 system.The reactivities of the resulting peroxycarbonic acids were compared.O-Trichloroethylperoxycarbonic acid prepared in this way was isolated as a chloroform solution and was characterized spectroscopically.KEYWORDS - oxygenation with 1-alkoxycarbonyl-1,2,4-triazole/H2O2 system; peroxycarbonic acid; epoxidation; Baeyer-Villiger reaction

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