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82410-79-5

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82410-79-5 Usage

Molecular structure

1H-Imidazole, 1,1'-[1,4-phenylenebis(methylene)]bis[2-methylis a chemical compound that consists of an imidazole ring with a phenylenebis(methylene) linkage and two methyl groups attached to the nitrogen atom.

Derivative

It is a derivative of imidazole.

Industrial applications

It is used as a building block in the synthesis of pharmaceuticals and agrochemicals.

Antimicrobial and antifungal properties

It has been studied for its potential antimicrobial and antifungal properties, making it a promising candidate for the development of new drug therapies.

Polymer production

It is used in the production of polymers and other materials due to its ability to enhance the stability and durability of the final products.

Check Digit Verification of cas no

The CAS Registry Mumber 82410-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,1 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82410-79:
(7*8)+(6*2)+(5*4)+(4*1)+(3*0)+(2*7)+(1*9)=115
115 % 10 = 5
So 82410-79-5 is a valid CAS Registry Number.

82410-79-5SDS

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 2-methyl-1-[[4-[(2-methylimidazol-1-yl)methyl]phenyl]methyl]imidazole

1.2 Other means of identification

Product number -
Other names 1H-Imidazole,1,1'-[1,4-phenylenebis(methylene)]bis[2-methyl

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:82410-79-5 SDS

82410-79-5Downstream Products

82410-79-5Relevant articles and documents

Supramolecular solvatochromism: Mechanistic insight from crystallography, spectroscopy and theory

Nikolayenko, Varvara I.,Van Wyk, Lisa M.,Munro, Orde Q.,Barbour, Leonard J.

, p. 6975 - 6978 (2018)

A solvatochromic dinuclear copper(ii) metallocycle effectively traps tetrahydrofuran, diethyl ether and pentane significantly above their boiling points. X-ray crystallography, EPR and UV-visible spectroscopy were used to delineate an empirical relationsh

Guest-induced conformational switching in a single crystal

Dobrzanska, Liliana,Lloyd, Gareth O.,Esterhuysen, Catharine,Barbour, Leonard J.

, p. 5856 - 5859 (2006)

Without destruction of monocrystallinity: The conformational switching of a dinuclear metal complex between four distinct states (see picture) occurs without destroying the single crystal. This observation implies a substantial degree of cooperativity bet

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