56408-70-9 Usage
Uses
Used in Pharmaceutical Industry:
Uracil is used as a component in the development of various anticancer drugs. Its presence in these drugs aids in the inhibition of cancer cell growth and the regulation of nucleic acid metabolism, making it a valuable compound in cancer treatment.
Used in Anti-HIV Therapy:
In the field of anti-HIV therapy, uracil is utilized as a component of some therapeutic agents. Its role in these treatments contributes to the suppression of the HIV virus, helping to manage the progression of the disease.
Used in Nucleic Acid Metabolism:
Uracil plays a crucial role in nucleic acid metabolism, serving as a substrate for enzymes involved in DNA replication and repair. Its presence in these biological processes is essential for maintaining the integrity and stability of genetic information.
Used in Research and Development:
Uracil is also used in research and development for the study of nucleic acid structure, function, and interactions. Its unique properties and role in biological systems make it a valuable tool for understanding the mechanisms of genetic information processing and regulation.
Check Digit Verification of cas no
The CAS Registry Mumber 56408-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,0 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56408-70:
(7*5)+(6*6)+(5*4)+(4*0)+(3*8)+(2*7)+(1*0)=129
129 % 10 = 9
So 56408-70-9 is a valid CAS Registry Number.
56408-70-9Relevant academic research and scientific papers
Goyal, Rajendra N.,Singhai, Naveen K.
, p. 199 - 207 (1998)
The electrochemical oxidation of 1,3-dimethylxanthine has been studied in the pH range 2.3 - 10.3 at a pyrolytic graphite electrode. The conjugate base has been found as the electroactive species oxidized over the entire pH range. The 4e, 4H+ charge transfer step is followed by competitive irreversible chemical reactions. The decomposition of UV-absorbing intermediate generated during the electrooxidation has been found to follow first-order kinetics. The products of the EC reaction have been separated by HPLC and gel-permeation chromatography and characterized by mp, 1HNMR, and mass spectra. The presence of methyl groups of positions 1 and 3 has been found to affect the course of mechanism, because the positive charge developed on nitrogen does not permit ring contraction. A tentative mechanism has also been suggested.
