77079-61-9

Basic information

• Product Name: C₁₆H₁₇BrN₇O₇P
• Synonyms: C₁₆H₁₇BrN₇O₇P
• CAS NO: 77079-61-9
• Molecular Weight: 530.231
• Mol File: 77079-61-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₆H₁₇BrN₇O₇P(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₆H₁₇BrN₇O₇P(77079-61-9)
• EPA Substance Registry System: C₁₆H₁₇BrN₇O₇P(77079-61-9)

Safety Data

• Hazardous Substances Data: 77079-61-9(Hazardous Substances Data)

Upstream product

• 61-19-8 5'-adenosine monophosphate 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 77079-62-0 C₁₆H₁₈N₇O₁₀PS 
• 77079-60-8 C₁₇H₂₀N₇O₇P 
• 77079-59-5 C₁₆H₁₈N₇O₇P 
• 77071-04-6 8-(4-bromophenyl)adenine 
• 61-19-8 5'-adenosine monophosphate 

Relevant articles and documents

Reactions of Benzenediazonium Ions with Adenine and Its Derivatives

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.