16952-45-7 Usage
Description
2-Methylpyrido[4,3-d]pyrimidin-4(3H)-one is a heterocyclic chemical compound with the molecular formula C8H7N3O, featuring a pyrido and a pyrimidin ring. It is widely recognized for its potential biological activities and versatile reactivity, making it a significant building block in the synthesis of pharmaceuticals and biologically active compounds. Its importance in medicinal chemistry and drug discovery is underscored by its potential therapeutic applications across various disease areas.
Uses
Used in Pharmaceutical Synthesis:
2-Methylpyrido[4,3-d]pyrimidin-4(3H)-one is used as a key building block for the synthesis of various pharmaceuticals and biologically active compounds, leveraging its unique structure and reactivity to create novel therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-Methylpyrido[4,3-d]pyrimidin-4(3H)-one is utilized as a lead compound for the development of new drugs, given its demonstrated potential in exhibiting biological activities that are relevant to treating different diseases.
Used in Anticancer Applications:
2-Methylpyrido[4,3-d]pyrimidin-4(3H)-one is employed as an anticancer agent, capitalizing on its potential to target and treat cancer cells, thereby contributing to the advancement of cancer therapeutics.
Used in Antimicrobial Applications:
2-Methylpyrido[4,3-d]pyrimidin-4(3H)-one is also used in antimicrobial applications, harnessing its ability to combat microbial infections, which is crucial in the development of new antibiotics and antifungal agents.
Used in Anti-inflammatory Applications:
2-Methylpyrido[4,3-d]pyrimidin-4(3H)-one is applied in anti-inflammatory research and treatment, potentially offering new avenues for managing inflammation-related conditions.
Used in Drug Discovery:
In the realm of drug discovery, 2-Methylpyrido[4,3-d]pyrimidin-4(3H)-one serves as a valuable compound for identifying and optimizing new molecular entities with therapeutic potential for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 16952-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,5 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16952-45:
(7*1)+(6*6)+(5*9)+(4*5)+(3*2)+(2*4)+(1*5)=127
127 % 10 = 7
So 16952-45-7 is a valid CAS Registry Number.
16952-45-7Relevant articles and documents
Dehydrogenation of 6-Azaquinazoline Derivatives. Formation of Unexpected Quinonediimine Intermediates
Huber, Imre,Fueloep, Ferenc,Lazar, Janos,Bernath, Gabor,Toth, Gabor
, p. 157 - 162 (2007/10/02)
2,6-Disubstituted 5,6,7,8-tetrahydropyridopyrimidin-4(3H)-one (6-azaquinazoline) derivatives 7a-e were synthesized from N-substituted 3-methoxycarbonyl-4-piperidones 5a, b and amidines 6a-c.Compounds 7a-d and the debenzylated derivatives 8a-c under
