7577-92-6 Usage
Uses
Used in Pharmaceutical Industry:
5-Methylaminouracil is used as a chemical intermediate for the development of antiviral and antineoplastic drugs, leveraging its unique structural properties to target specific biological processes and pathways.
Used in Biochemical Research:
In the field of biochemistry, 5-Methylaminouracil serves as a research compound to investigate the structure and function of nucleic acids, contributing to a deeper understanding of genetic material and its interactions.
Used in Genetic Engineering and Molecular Biology:
5-Methylaminouracil is utilized as a molecular tool in genetic engineering and molecular biology research, potentially aiding in the manipulation and study of genetic information, thus advancing the development of novel biotechnological applications and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 7577-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7577-92:
(6*7)+(5*5)+(4*7)+(3*7)+(2*9)+(1*2)=136
136 % 10 = 6
So 7577-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H7N3O2/c1-6-3-2-7-5(10)8-4(3)9/h2,6H,1H3,(H2,7,8,9,10)
7577-92-6Relevant academic research and scientific papers
Photochemical reactions of 5-fluoropyrimidine bases with selected alkylamines
Kanciurzewska, Anna,Raczkowski, Mateusz,Ciszewski, Krzysztof,Celewicz, Lech
, p. 761 - 763 (2007/10/03)
Novel photochemical reactions between 5-fluoropyrimidine bases and primary alkylamines are described. Photoreaction of 5-fluorouracil with alkylamines in aqueous solution (pH>8) leads to 5-alkylaminouracils as the main photoproducts. Similarly, photoreact
