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40322-21-2

1H-1,2,4-Triazole-1-carboxylicacid,ethylester(6CI,7CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40322-21-2

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40322-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40322-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,2 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40322-21:
(7*4)+(6*0)+(5*3)+(4*2)+(3*2)+(2*2)+(1*1)=62
62 % 10 = 2
So 40322-21-2 is a valid CAS Registry Number.

40322-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1H-1,2,4-triazole-1-carboxylate

1.2 Other means of identification

Product number -
Other names [1,2,4]triazole-1-carboxylic acid ethyl ester

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:40322-21-2 SDS

40322-21-2Relevant articles and documents

Chemoselective N-acylation of indoles and oxazolidinones with carbonylazoles

Heller, Stephen T.,Schultz, Erica E.,Sarpong, Richmond

supporting information; experimental part, p. 8304 - 8308 (2012/09/08)

Unique reactivity: In the presence of more reactive amine and alcohol functional groups and of carboxylic acids, the chemoselective N-acylation of indoles (see scheme) and oxazolidinones is achieved by taking advantage of the unique reactivity of carbonylazole acylating agents with catalytic amounts of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Copyright

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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