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ETHYL 1-METHYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39039-48-0

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39039-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39039-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,3 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39039-48:
(7*3)+(6*9)+(5*0)+(4*3)+(3*9)+(2*4)+(1*8)=130
130 % 10 = 0
So 39039-48-0 is a valid CAS Registry Number.

39039-48-0SDS

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 1-methyltriazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 1-methyl-1H-1,2,3-triazole-4-carboxylate

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:39039-48-0 SDS

39039-48-0Relevant academic research and scientific papers

Regioselective synthesis of 1,4-disubstituted triazoles using bis[(L)prolinato-N,O]Zn complex as an efficient catalyst in water as a sole solvent

Kidwai, Mazaahir,Jain, Arti

experimental part, p. 620 - 625 (2011/10/18)

A concise, convenient and mild route for one-pot regioselective synthesis of N-aryl- and N-alkyltriazoles in water as a sole solvent is reported. The methodology involves a three-component reaction comprising aryl/alkyl-alkyne, sodium azide and aryl/alkyl

Study of the reactivity of nitriles towards diazomethane: synthesis and structural study of N-methyl-v-triazoles

Danoun, Saida,Baziard-Mouysset, Genevieve,Stigliani, Jean-Luc,Commenges, Gerard,Carpy, Alain,Payard, Marc

, p. 943 - 951 (2007/10/02)

In this work, we examined the effect of diazomethane on 12 nitriles.Five gave rise to three isomeric N-methyl-v-triazoles, which were isolated.Their structural features were established and, in one case, corroborated by X-ray analysis.A generalization of the structural attribution by 13C NMR is proposed.A study of the electronic distribution was carried out for a total 17 nitriles and helped establish a predictive criterion of their reactivity towards diazomethane. diazomethane / nitrile / v-triazole / electronic density

Heterocyclic-methylene-penems

-

, (2008/06/13)

(5R) (Z)-6-(1-methyl,1,2,3-triazol-4-yl-methylene)-penem-3-carboxylic acid and its salts are provided in analytically pure crystalline form, and the salts in hydrated form, for example (5R) sodium (Z)-6-(1-methyl-1,2,3-triazol-4-yl-methylene)penem-3-carboxylate monohydrate.

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