77071-04-6 Usage
Uses
Used in Pharmaceutical Research:
8-(4-bromophenyl)-7H-purin-6-amine is used as a research compound for exploring its potential biological activity and interactions with various biological targets. Its structural similarity to other purine-based compounds suggests that it may have therapeutic applications in treating certain diseases or conditions.
Used in Drug Development:
8-(4-bromophenyl)-7H-purin-6-amine is used as a starting material or intermediate in the synthesis of new drugs. Its unique properties, including the bromophenyl substitution, may allow for the development of novel therapeutic agents with improved efficacy, selectivity, or reduced side effects compared to existing treatments.
Used in Chemical Reactions:
8-(4-bromophenyl)-7H-purin-6-amine is used as a reactant in various chemical reactions to modify its structure or functionalize it with other chemical groups. This can lead to the creation of new compounds with different properties and potential applications in various fields, including materials science, diagnostics, or therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 77071-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,7 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 77071-04:
(7*7)+(6*7)+(5*0)+(4*7)+(3*1)+(2*0)+(1*4)=126
126 % 10 = 6
So 77071-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H8BrN5/c12-7-3-1-6(2-4-7)10-16-8-9(13)14-5-15-11(8)17-10/h1-5H,(H3,13,14,15,16,17)
77071-04-6Relevant academic research and scientific papers
Reactions of Benzenediazonium Ions with Adenine and Its Derivatives
Chin, Anton,Hung, Ming-Hong,Stock, Leon M.
, p. 2203 - 2207 (2007/10/02)
Adenine, adenosine, and 5'-adenylic acid react readily with benzenediazonium ion and its derivatives at pH 8-11 to yield derivatives of (E)-6-(3-phenyl-2-triazen-1-yl)purine.The structural assignments for these compounds, some of which are unstable, are based on their spectroscopic properties and their degradation reactions in acid solution and with sodium dithionite to yield 6-hydrazinopurine.The triazenes decompose in basic aqueous solution at 60-90 deg C to produce 8-aryladenines.For adenosine and 5'-adenylic acid, the ribose residues are cleaved during this process.Several lines of evidence indicate that the triazenes are converted to 8-aryladenines in intermolecular processes.Both the benzenediazonium ion and the phenyl radical can be intercepted during the reaction.Consequently, the phenylation reaction may be confidently formulated as an intermolecular free-radical substitution reaction.
