35779-39-6 Usage
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 academic research and scientific papers
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.
One-step direct conversion of heterocyelie aldehydes to esters
Goswami, Shyamaprosad,Hazra, Anita
supporting information; experimental part, p. 484 - 485 (2010/03/04)
One-step direct conversion of a series of heteroeyelie aldehydes to heterocyclie esters is reported here by the use of thiamine hydrochloride as a catalyst in the absence of nitrogen atmosphere in a reasonably high yield. This method exclusively produces
