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CAS 2140-25-2

:

9-(5-O-acetylpentofuranosyl)-9H-purin-6-amine

Description:
9-(5-O-acetylpentofuranosyl)-9H-purin-6-amine, also known by its CAS number 2140-25-2, is a purine derivative characterized by the presence of a purine base linked to a furanosyl sugar moiety. This compound features an acetyl group at the 5-position of the sugar, which can influence its solubility and biological activity. The purine structure is essential in various biological processes, including nucleic acid synthesis and energy transfer, as it is a component of nucleotides. The presence of the amine group at the 6-position of the purine ring contributes to its reactivity and potential interactions with other biomolecules. This compound may exhibit specific pharmacological properties, making it of interest in medicinal chemistry and biochemistry. Its structural characteristics suggest potential applications in research related to nucleoside analogs, which can be important in the development of antiviral and anticancer agents. Overall, the unique combination of the sugar and purine components in this molecule contributes to its functional versatility in biological systems.
Formula:C12H15N5O5
InChI:InChI=1/C12H15N5O5/c1-5(18)21-2-6-8(19)9(20)12(22-6)17-4-16-7-10(13)14-3-15-11(7)17/h3-4,6,8-9,12,19-20H,2H2,1H3,(H2,13,14,15)
SMILES:CC(=O)OCC1C(C(C(n2cnc3c(N)ncnc23)O1)O)O
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Found 3 products.
  • 5''-O-Acetyladenosine
    Glentham
    + Info

    5''-O-Acetyladenosine

    CAS:
    Formula:C12H15N5O5
    Molecular weight:309.28

    Ref: 7W-GN4346

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  • 5'-O-Acetyladenosine
    Biosynth
    + Info

    5'-O-Acetyladenosine

    CAS:
    <p>5'-O-Acetyladenosine is a labile nucleoside that can be converted to adenosine. It is a substrate for the enzyme ribonucleotide reductase, which converts it to adenosine monophosphate. 5'-O-Acetyladenosine has been shown to function as an equilibrating agent in the synthesis of guanosine and other pyrimidine nucleotides. In addition, it is a precursor for the synthesis of purines. 5'-O-Acetyladenosine can be synthesized from trimethyl phosphate and chloride gas yields acetaldehyde, which then reacts with phosphorus oxychloride to form 5'-O-acetyladeninol, which undergoes hydrolysis to yield 5'-O-acetyladenosine. The regioselectivity of this reaction depends on the concentration of reactants and solvents used in the reaction.</p>
    Formula:C12H15N5O5
    Purity:Min. 95%
    Color and Shape:White Powder
    Molecular weight:309.28 g/mol

    Ref: 3D-NA09588

    1g
    962.00€
    50mg
    204.00€
    100mg
    305.00€
    250mg
    477.00€
    500mg
    681.00€
  • 5'-O-Acetyl Adenosine
    TRC
    + Info

    5'-O-Acetyl Adenosine

    Controlled Product
    CAS:
    <p>Applications Adenosine derivative.<br>References Bloch, A., et al.: J. Med. Chem., 10, 908 (1967), Wilson, D., et al.: Biochemistry, 32, 1689 (1993), Ferrero, M., et al.: Chem. Rev., 100, 4319 (2000),<br></p>
    Formula:C12H15N5O5
    Color and Shape:Neat
    Molecular weight:309.28

    Ref: TR-A168060

    50mg
    290.00€
    500mg
    1,940.00€