77071-04-6 Usage
General Description
8-(4-bromophenyl)-7H-purin-6-amine is a chemical compound with a purine core structure and a bromophenyl substitution. It is also known as 4-Bromo-8-(4-bromophenyl)-7H-purine-6-amine and has a molecular formula of C11H8Br2N6. 8-(4-bromophenyl)-7H-purin-6-amine is a derivative of purine, a naturally occurring organic compound present in DNA, RNA, and other biological molecules. It may have potential applications in pharmaceutical research and drug development due to its structural similarity to other purine-based compounds, which are known to have biological activity in the human body. The bromophenyl substitution adds unique properties to this compound and could make it suitable for specific chemical reactions or interactions with biological targets. Overall, 8-(4-bromophenyl)-7H-purin-6-amine is an interesting chemical compound with potential scientific and pharmaceutical applications.
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 articles and documents
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.
