88508-72-9 Usage
Uses
Used in Pharmaceutical Research:
2,6-dimethoxy-9-pentofuranosyl-9H-purine is used as a research compound for exploring its biological activities and potential medicinal uses. Its unique structure makes it a promising candidate for the development of new therapeutic agents.
Used in Anti-viral Applications:
In the field of anti-viral research, 2,6-dimethoxy-9-pentofuranosyl-9H-purine is used as a potential therapeutic agent to combat viral infections. Its specific interactions with viral components may offer novel approaches to treating viral diseases.
Used in Anti-cancer Applications:
2,6-dimethoxy-9-pentofuranosyl-9H-purine is also utilized as an anti-cancer agent in research settings. Its potential to interfere with cancer cell processes and its unique chemical properties make it a candidate for further investigation into its role in cancer treatment.
Used in Biochemical Research:
2,6-dimethoxy-9-pentofuranosyl-9H-purine serves as a valuable tool in biochemical research, aiding scientists in understanding the mechanisms of nucleoside metabolism and the role of purine bases in various biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 88508-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,0 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88508-72:
(7*8)+(6*8)+(5*5)+(4*0)+(3*8)+(2*7)+(1*2)=169
169 % 10 = 9
So 88508-72-9 is a valid CAS Registry Number.
88508-72-9Relevant academic research and scientific papers
A new method for synthesis of 2-alkoxyadenosine analogs
Sakakibara, Norikazu,Tsuruta, Takashi,Komatsu, Masahiro,Iwai, Masatoshi,Maruyama, Tokumi
experimental part, p. 2299 - 2311 (2011/11/06)
O6-Methylguanosine and 2-amino-6-chloropurine riboside derivative were treated with isoamylnitrite in the presence of an appropriate alcohol to give the corresponding 2-alkoxy-6-methoxy (or chloro) purine riboside derivatives.
IMPROVED SYNTHESIS OF 2-SUBSTITUTED ADENOSINES
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Page/Page column 14-15, (2008/06/13)
A method of synthesis of a 2-substituted adenosine of formula I which comprises converting a compound of formula II to a compound of formula (I), wherein: R is C 1-6 alkoxy (straight or branched), a phenoxy group (unsubstituted, or mono-, or di-substituted by halo, amino, CF3-, cyano, nitro, C 1-6 alkyl, or C 1-6 alkoxy), a benzyloxy group (unsubstituted, or mono-, or di-substituted by halo, amino, CF3-, cyano, nitro, Cl_6 alkyl, or Cl_6 alkoxy), or a benzoyl group (unsubstituted, or mono-, or di-substituted by halo, amino, CF3-, cyano, nitro, C 1-6 alkyl, or C 1-6 alkoxy); R' = H, or a protecting group.
