84331-29-3 Usage
Molecular Structure
A purine analog with two amino groups at the 2 and 6 positions and a ketone group at the 1 position.
Derivation
Derived from the purine base.
Biological Activity
Selective inhibitor of dopamine beta-hydroxylase, an enzyme involved in the synthesis of norepinephrine.
Potential Use
Treatment of conditions such as hypertension and renal failure.
Antimicrobial Properties
Has shown potential as an antiviral, antifungal, and antibacterial agent.
Pharmaceutical Development
Studied for its potential use in the development of new pharmaceuticals and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 84331-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,3 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84331-29:
(7*8)+(6*4)+(5*3)+(4*3)+(3*1)+(2*2)+(1*9)=123
123 % 10 = 3
So 84331-29-3 is a valid CAS Registry Number.
84331-29-3Relevant academic research and scientific papers
Tang, Yongxing,Li, Kejia,Chinnam, Ajay Kumar,Staples, Richard J.,Shreeve, Jean'ne M.
, p. 2143 - 2148 (2021)
Three nitrogen-rich heterocyclic compounds containing the diamino-pyrimidine mono-N-oxide moiety were synthesizedviamild oxidation reactions. Oxidation of the furazano-pyrimidine compound (1) with a mixture of trifluoroacetic anhydride (TFAA) and hydrogen peroxide (50%) gave the nitrate salt (3). All of the compounds were characterized by NMR spectra, elemental analysis, and single-crystal X-ray diffraction. They show high thermal stability and good detonation performance as well as low sensitivity.
