24466-52-2 Usage
Uses
Used in Pharmaceutical Industry:
1-Propylpyrimidine-2,4(1H,3H)-dione is used as an antiviral agent for the treatment of viral infections such as herpes, influenza, and hepatitis. Its antiviral properties make it a valuable component in managing and treating these infections.
1-Propylpyrimidine-2,4(1H,3H)-dione is also used as an immunomodulatory agent, which helps regulate the immune system's response to various conditions. This property is beneficial in the treatment of autoimmune diseases, where the immune system mistakenly attacks the body's own tissues.
Furthermore, 1-Propylpyrimidine-2,4(1H,3H)-dione is used as an anti-inflammatory agent, reducing inflammation and alleviating symptoms associated with inflammatory conditions.
In addition to its current applications, 1-Propylpyrimidine-2,4(1H,3H)-dione is being studied for its potential as an anti-cancer agent. Its ability to target and inhibit the growth of cancer cells is a promising area of research, with the potential to contribute to cancer treatment strategies.
However, further research is needed to fully understand and utilize the therapeutic potential of 1-Propylpyrimidine-2,4(1H,3H)-dione in various medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 24466-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,6 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24466-52:
(7*2)+(6*4)+(5*4)+(4*6)+(3*6)+(2*5)+(1*2)=112
112 % 10 = 2
So 24466-52-2 is a valid CAS Registry Number.
24466-52-2Relevant academic research and scientific papers
Ammonium formate/palladium on carbon: A versatile system for catalytic hydrogen transfer reductions of carbon-carbon double bonds
Paryzek, Zdzislaw,Koenig, Hanna,Tabaczka, Bartlomiej
, p. 2023 - 2026 (2007/10/03)
Various carbon-carbon double bonds in olefins and α,β -unsaturated ketones were effectively reduced to the corresponding alkanes and saturated ketones, using ammonium formate as a hydrogen transfer agent in the presence of Pd/C as catalyst in refluxing methanol.
Synthesis by conjugate radical addition of new heterocyclic amino acids with nucleic acid bases in their side chains
Jones,Berthelot,Iley
, p. 2131 - 2132 (2007/10/03)
N-(2-Iodoethyl) and N-(3-iodopropyl)pyrimidines and purines undergo stereoselective conjugate radical addition with an optically active oxazolidinone acceptor to give syn-adducts that can be converted into pyrimidine and purine amino acids.
