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6950-04-5

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6950-04-5 Usage

General Description

1,2-Di-(4-pyridyl)-1,2-ethanediol is a chemical compound with the formula C12H12N2O2. It is a derivative of ethylene glycol and consists of two pyridine rings attached to the ethylene backbone. 1 2-DI-(4-PYRIDYL)-1 2-ETHANEDIOL is often used as a chelating agent in coordination chemistry and as a building block for the synthesis of various organic compounds. It has also been studied for its potential use in pharmaceuticals and as a precursor for the synthesis of coordination polymers. Additionally, 1,2-Di-(4-pyridyl)-1,2-ethanediol has demonstrated antioxidant properties, making it of interest for potential applications in the food and cosmetic industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6950-04-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6950-04:
(6*6)+(5*9)+(4*5)+(3*0)+(2*0)+(1*4)=105
105 % 10 = 5
So 6950-04-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2/c15-11(9-1-5-13-6-2-9)12(16)10-3-7-14-8-4-10/h1-8,11-12,15-16H

6950-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Di-4-pyridinyl-1,2-ethanediol

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

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More Details:6950-04-5 SDS

6950-04-5Relevant articles and documents

REDUCTIVE REACTIONS OF SUBSTITUTED PYRIDINES BY AQUEOUS TITANIUM TRICHLORIDE

Clerici, Angelo,Porta, Ombretta

, p. 1293 - 1297 (2007/10/02)

Aqueous titanium trichloride reductively removes cyano and halo groups from the correspondingly substituted pyridines by a two electron-transfer process and promotes reduction of pyridyl-ketones and aldehydes to glycols by one electron-transfer process under very simple experimental conditions.

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