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CAS 6612-73-3

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3'-O-acetyl-2'-deoxyadenosine

Description:
3'-O-acetyl-2'-deoxyadenosine is a modified nucleoside that features an acetyl group at the 3' position of the ribose sugar, which is a characteristic modification that can influence its biochemical properties. This compound is a derivative of 2'-deoxyadenosine, a building block of DNA, and is often used in biochemical research and synthesis. The acetylation can enhance the stability of the nucleoside and alter its interactions with enzymes and other biomolecules. It is typically soluble in polar organic solvents and may exhibit different reactivity compared to its unmodified counterpart. The presence of the acetyl group can also affect its ability to participate in hydrogen bonding and base pairing, which is crucial for its role in nucleic acid chemistry. Additionally, 3'-O-acetyl-2'-deoxyadenosine may serve as a useful intermediate in the synthesis of more complex nucleoside analogs or in the study of nucleic acid structure and function. Its CAS number, 6612-73-3, is a unique identifier that facilitates its identification in chemical databases and literature.
Formula:C12H15N5O4
InChI:InChI=1/C12H15N5O4/c1-6(19)20-7-2-9(21-8(7)3-18)17-5-16-10-11(13)14-4-15-12(10)17/h4-5,7-9,18H,2-3H2,1H3,(H2,13,14,15)
SMILES:CC(=O)OC1CC(n2cnc3c(N)ncnc23)OC1CO
Synonyms:
  • 9-(3-O-acetyl-2-deoxypentofuranosyl)-9H-purin-6-amine
  • Adenosine, 2'-deoxy-, 3'-acetate
  • 3'-O-Ac-dA
  • 3'-O-ACETYL-2'-DEOXYADENOSINE
  • 2'-Deoxyadenosine 3'-acetate
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