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35779-39-6

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35779-39-6 Usage

General Description

1,2-di(pyridin-3-yl)ethane-1,2-dione, also known as acetylpyridinium, is a chemical compound with the molecular formula C12H9NO2. It is a derivative of the organic compound pyridine, with two pyridine rings attached to a central ethane-1,2-dione structure. 1,2-di(pyridin-3-yl)ethane-1,2-dione is commonly used as a precursor in the synthesis of heterocyclic compounds and pharmaceuticals due to its versatile reactivity. Acetylation and reduction reactions of 1,2-di(pyridin-3-yl)ethane-1,2-dione have also been studied for their potential applications in organic synthesis. Additionally, it has been investigated for its antibacterial and antifungal properties, making it a potential candidate for use in medical and antimicrobial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 35779-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,7 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35779-39:
(7*3)+(6*5)+(5*7)+(4*7)+(3*9)+(2*3)+(1*9)=156
156 % 10 = 6
So 35779-39-6 is a valid CAS Registry Number.

35779-39-6SDS

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-dipyridin-3-ylethane-1,2-dione

1.2 Other means of identification

Product number -
Other names HMS2782O20

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:35779-39-6 SDS

35779-39-6Downstream Products

35779-39-6Relevant articles and documents

Electrochemical Oxidation of Alcohols and Aldehydes to Carboxylic Acids Catalyzed by 4-Acetamido-TEMPO: An Alternative to "anelli" and "pinnick" Oxidations

Rafiee, Mohammad,Konz, Zachary M.,Graaf, Matthew D.,Koolman, Hannes F.,Stahl, Shannon S.

, p. 6738 - 6744 (2018/06/19)

An electrocatalytic method has been developed to oxidize primary alcohols and aldehydes to the corresponding carboxylic acids using 4-acetamido-2,2,6,6-tetramethylpiperidin-1-oxyl (ACT) as a mediator. The method successfully converts benzylic, aliphatic, heterocyclic, and other heteroatom-containing substrates to the corresponding carboxylic acids in aqueous solution at room temperature. The mild conditions enable retention of stereochemistry adjacent to the site of oxidation, as demonstrated in a 40 g-scale synthesis of a precursor to levetiracetam, a medication used to treat epilepsy.

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