35779-39-6 Usage
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 known for its versatile reactivity, making it a valuable precursor in the synthesis of heterocyclic compounds and pharmaceuticals.
Uses
Used in Pharmaceutical Synthesis:
1,2-di(pyridin-3-yl)ethane-1,2-dione is used as a precursor in the pharmaceutical industry for the synthesis of heterocyclic compounds and pharmaceuticals. Its unique structure and reactivity allow for the creation of a wide range of therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 1,2-di(pyridin-3-yl)ethane-1,2-dione is utilized as a versatile building block. Its acetylation and reduction reactions have been studied for their potential applications in creating new organic compounds.
Used in Medical and Antimicrobial Applications:
1,2-di(pyridin-3-yl)ethane-1,2-dione has been investigated for its antibacterial and antifungal properties. These characteristics make it a potential candidate for use in medical applications, particularly in the development of new antimicrobial agents to combat resistant strains of bacteria and fungi.
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.
35779-39-6Relevant 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.
