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1,2-Ethanedione, 1,2-di-2-quinolinyl, also known as 1,2-diquinolylethylene, is an organic compound with the chemical formula C18H12N2O2. It is a derivative of ethanedione (glyoxal), where two 2-quinolyl groups are attached to the central carbon atoms. This molecule is characterized by its conjugated π-system, which extends across the entire molecule, providing it with unique electronic properties. It is often used in the synthesis of various organic compounds and as a building block in the creation of more complex molecules, particularly in the field of heterocyclic chemistry. The compound is known for its stability and can be used in the formation of metal complexes, which have potential applications in materials science and medicinal chemistry.

3561-22-6

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3561-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3561-22-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3561-22:
(6*3)+(5*5)+(4*6)+(3*1)+(2*2)+(1*2)=76
76 % 10 = 6
So 3561-22-6 is a valid CAS Registry Number.

3561-22-6SDS

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-(2',2'')-diquinolylethanedione

1.2 Other means of identification

Product number -
Other names 2,2'-quinadil

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:3561-22-6 SDS

3561-22-6Relevant academic research and scientific papers

Improved oxidation of active methyl group of N-heteroaromatic compounds by selenium dioxide in the presence of tert-butyl hydroperoxide

Tagawa, Yoshinobu,Yamashita, Katsuya,Higuchi, Yoshitaka,Goto, Yoshinobu

, p. 953 - 957 (2007/10/03)

The oxidation of active methyl group of N-heteroaromatic compounds including both of bicyclic and monocyclic compounds using SeO2 was considerably improved in the presence of tert-butyl hydroperoxde in dioxane to give the corresponding aldehyde or carboxylic acid in the moderate to good yields. The present oxidation proceeds more mildly and more selectively to form aldehyde rather than carboxylic acid, compared with conventional SeO2 oxidation without tert-butyl hydroperoxide.

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