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1-benzyl-4,5-bis(chloromethyl)-1H-1,2,3-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70691-95-1

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70691-95-1 Usage

Structure

A triazole derivative with two chloromethyl groups attached to the 4 and 5 positions of the triazole ring, and a benzyl group attached to the 1 position.

Application

Commonly used in organic chemistry for the synthesis of various pharmaceuticals and agrochemicals.

Potential

Has potential applications in medicinal chemistry due to its unique structure and potential biological activities.

Use

Can be used as a building block for the preparation of new compounds with diverse properties.

Check Digit Verification of cas no

The CAS Registry Mumber 70691-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,9 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70691-95:
(7*7)+(6*0)+(5*6)+(4*9)+(3*1)+(2*9)+(1*5)=141
141 % 10 = 1
So 70691-95-1 is a valid CAS Registry Number.

70691-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4,5-bis(chloromethyl)triazole

1.2 Other means of identification

Product number -
Other names 1-Benzyl-4,5-bis-chlormethyl-1H-1,2,3-triazol

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:70691-95-1 SDS

70691-95-1Relevant academic research and scientific papers

Continuous-flow azide-alkyne cycloadditions with an effective bimetallic catalyst and a simple scavenger system

?tv?s, Sndor B.,Hatoss, Gbor,Georgides, dm,Kovcs, Szabolcs,Mndity, Istvn M.,Novk, Zoltn,Fül?p, Ferenc

, p. 46666 - 46674 (2014/12/10)

A flow chemistry-based technique is presented herein for Cu(i)-catalyzed azide-alkyne cycloadditions with a copper on iron bimetallic system as the catalyst and iron powder as a readily available copper scavenger. The method proved to be rapid and safe as

Synthesis of noncondensed polynuclear vicinal triazoles

Tikhonova,Serebryakova,Maksikova,Gareev,Vereshchagin

, p. 1241 - 1244 (2007/10/02)

The reaction of propargyl alcohol and butynediol with organic mono- and diazides gave N-alkyl-C-hydroxymethyl-1,2,3-triazoles, the hydroxy group of which was transformed successively to a halo group and an azide fragment. Two- and three-ring triazole stru

UNSATURATED CARBONYL-CONTAINING COMPOUNDS. XXVIII. CYCLOADDITION OF ORGANIC AZIDES TO α-ACETYLENIC KETONES AND ACIDS

Vereshchagin, L. I.,Tikhonova, L. G.,Maksikova, A. V.,Serebryakova, E. S.,Proidakov, A. G.,Filippova, T. M.

, p. 641 - 648 (2007/10/02)

The reaction of α-acetylenic ketones and acids with organic azides leads to the formation of 1-alkyl(aryl)-4-acyl(carboxy)-1,2,3-triazoles or to a mixture of the 1,4- and 1,5-disubstituted isomers.The effect of the structure of the initial compound and of the solvent on the direction of cycloaddition was investigated.

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