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1,2-Benzenediamine, N,N,N'-tris(2-pyridinylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142991-51-3

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142991-51-3 Usage

Type of compound

Chelating agent

Usage

Research and laboratory settings

Structure

Tridentate ligand with three pyridine groups

Function

Binds to metal ions and forms stable complexes

Affinity

High affinity for zinc

Application

Chelates and removes zinc from biological samples

Therapeutic potential

Conditions involving zinc dysregulation (e.g., cancer, neurodegenerative diseases)

Additional property

Antioxidant properties

Field of interest

Oxidative stress research

Considerations

Potential toxicity and non-selective binding to other metal ions in experimental and clinical settings

Check Digit Verification of cas no

The CAS Registry Mumber 142991-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,9,9 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 142991-51:
(8*1)+(7*4)+(6*2)+(5*9)+(4*9)+(3*1)+(2*5)+(1*1)=143
143 % 10 = 3
So 142991-51-3 is a valid CAS Registry Number.

142991-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,2-N,2-N-tris(pyridin-2-ylmethyl)benzene-1,2-diamine

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

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

More Details:142991-51-3 SDS

142991-51-3Downstream Products

142991-51-3Relevant academic research and scientific papers

Ligand transformations and efficient proton/water reduction with cobalt catalysts based on pentadentate pyridine-rich environments

Basu, Debashis,Mazumder, Shivnath,Shi, Xuetao,Baydoun, Habib,Niklas, Jens,Poluektov, Oleg,Schlegel, H. Bernhard,Verani, Cludio N.

, p. 2105 - 2110 (2015)

A series of cobalt complexes with pentadentate pyridine-rich ligands is studied. An initial CoII amine complex 1 is prone to aerial oxidation yielding a CoIII imine complex 2 that is further converted into an amide complex 4 in presence of adventitious water. Introduction of an N-methyl protecting group to the ligand inhibits this oxidation and gives rise to the CoII species 5. Both the CoIII 4 and CoII 5 show electrocatalytic H2 generation in weakly acidic media as well as in water. Mechanisms of catalysis seem to involve the protonation of a CoII-H species generated in situ.

Convenient synthesis of N,N,N',N'-tetrakis(2-pyridylmethyl)-α,ω-alkanediamines using a phase-transfer catalyst

Sato,Mori,Iida

, p. 539 - 540 (2007/10/02)

Alkylation of α,ω-alkanediamines and their N,N-disubstituted derivatives with 2-(chloromethyl)pyridinium chloride in the presence of hexadecyltrimethylammonium chloride as a phase-transfer catalyst gave conveniently the corresponding N,N,N',N'-tetrakis(2-

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