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3,5-dibenzyl-4H-1,2,4-triazol-4-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17591-59-2

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17591-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17591-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,9 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17591-59:
(7*1)+(6*7)+(5*5)+(4*9)+(3*1)+(2*5)+(1*9)=132
132 % 10 = 2
So 17591-59-2 is a valid CAS Registry Number.

17591-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dibenzyl-1,2,4-triazol-4-amine

1.2 Other means of identification

Product number -
Other names 3,5-Dibenzyl-[1,2,4]triazol-4-ylamin

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:17591-59-2 SDS

17591-59-2Downstream Products

17591-59-2Relevant academic research and scientific papers

Microwave-assisted synthesis of 3,5-Dibenzyl-4-amino-1,2,4-triazole and its diazo ligand, metal complexes along with anticancer activity

Jha, Anjali,Murthy,Durga,Sundari

experimental part, p. 1571 - 1577 (2011/12/22)

Synthesis of 3,5-dibenzyl-4-amino-1,2,4-triazole was accomplished via a conventional method as well as microwave irradiation method, followed by diazotization and coupling with 2,4-pentanedione. The dinucleating ligand was isolated and complexed with Ni(II), Cu(II) and Ru(III) chlorides. These complexes were screened on Jurkat, Raji & PBMC cell lines for anticancer activity. Ruthenium complexes showed potential anticancer activities.

Process for the synthesis of 4-amino-1,2,4-(4h)triazole derivatives

-

, (2008/06/13)

A process for preparing a 4-amino-1,2,4-(4H)triazole derivative compositions having the formula STR1 wherein R is hydrogen or an alkyl group containing from 1 to about 10 carbon atoms, which alkyl group can be additionally substituted by one or more aryl, heteroaryl, hydroxy, or alkenyl substituents, comprising the step of reacting hydrazine or an aqueous hydrazine solution with a carboxylic acid having the formula RCO2 H in the presence of an insoluble polymer containing acidic functional groups sufficiently strong to cause the reaction to proceed under mild conditions to produce a product of high yield and purity.

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