6220-50-4 Usage
Description
2(1H)-Pyrimidinone, 4-amino-6-methyl(9CI) is a chemical compound with the molecular formula C5H6N2O. It is a derivative of pyrimidine and is known for its potential antiviral and anticancer activity. 2(1H)-Pyrimidinone, 4-amino-6-methyl(9CI) is utilized in various pharmaceutical applications due to its structural and functional properties, and it plays a role in the synthesis of medicinal products. Its potential in the development of new drugs and therapies for a range of medical conditions is also being explored.
Uses
Used in Pharmaceutical Industry:
2(1H)-Pyrimidinone, 4-amino-6-methyl(9CI) is used as an intermediate in the synthesis of various medicinal products. Its unique structural properties make it a valuable component in the creation of new pharmaceutical compounds.
Used in Antiviral Applications:
2(1H)-Pyrimidinone, 4-amino-6-methyl(9CI) has been studied for its potential antiviral activity, making it a candidate for use in antiviral medications. Its ability to combat viruses could lead to the development of new treatments for viral infections.
Used in Anticancer Applications:
2(1H)-Pyrimidinone, 4-amino-6-methyl(9CI) is also being investigated for its potential anticancer properties. Its use in this area could contribute to the development of new cancer therapies and treatments.
Used in Drug Development:
2(1H)-Pyrimidinone, 4-amino-6-methyl(9CI) may have applications in the development of new drugs and therapies for a range of medical conditions. Its versatility and potential for various applications make it a promising candidate for further research and development in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 6220-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6220-50:
(6*6)+(5*2)+(4*2)+(3*0)+(2*5)+(1*0)=64
64 % 10 = 4
So 6220-50-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H7N3O/c1-3-2-4(6)8-5(9)7-3/h2H,1H3,(H3,6,7,8,9)
6220-50-4Relevant articles and documents
Reactions of pyrimidine nucleosides with aqueous alkalies: kinetics and mechanisms.
L?nnberg,Suokas,K?ppi,Darzynkiewicz
, p. 798 - 805 (2007/10/02)
Kinetics for the reactions of various cytosine and uracil nucleosides and their alkyl derivatives with aqueous sodium hydroxide have been studied by liquid chromatography. Blocking of the glycosyl hydroxyl groups with alkyl groups and changes in the glycon moiety configuration have been observed to exert only moderate effects on the rate of deamination of cytosine nucleosides. Methylation of the 4-amino group retards deamination considerably, while a methyl substituent at C5 is rate accelerating and at C6 only moderately rate retarding. These findings have been accounted for by a mechanism involving a rate limiting bimolecular displacement of the 4-amino group by a hydroxide ion. Analogous comparisons with uracil nucleosides suggest that the decomposition of uridine is initiated by an intermolecular attack of hydroxide ion on the C5 atom of the base moiety. In contrast, beta-D-arabino- and beta-D-lyxo-furanosyl derivatives appear to be cleaved via an intramolecular nucleophilic attack of the ionized 2'-hydroxyl group.
