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CAS 3056-18-6

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2,6-dichloro-9-(2,3,5-tri-O-acetylpentofuranosyl)-9H-purine

Description:
2,6-Dichloro-9-(2,3,5-tri-O-acetylpentofuranosyl)-9H-purine, with CAS number 3056-18-6, is a purine derivative characterized by the presence of two chlorine atoms at the 2 and 6 positions of the purine ring and a pentofuranosyl moiety that is fully acetylated at the 2', 3', and 5' hydroxyl groups. This compound exhibits properties typical of nucleosides, including potential biological activity due to its structural similarity to natural nucleosides. The acetyl groups enhance its lipophilicity, which may influence its absorption and distribution in biological systems. The dichloro substitution can affect its reactivity and interaction with biological targets, potentially impacting its pharmacological properties. As a synthetic compound, it may be used in research related to nucleic acid chemistry, antiviral drug development, or as a biochemical probe. Its stability, solubility, and reactivity would depend on the specific conditions of use, including pH and solvent environment.
Formula:C16H16Cl2N4O7
InChI:InChI=1/C16H16Cl2N4O7/c1-6(23)26-4-9-11(27-7(2)24)12(28-8(3)25)15(29-9)22-5-19-10-13(17)20-16(18)21-14(10)22/h5,9,11-12,15H,4H2,1-3H3
SMILES:CC(=O)OCC1C(C(C(n2cnc3c(Cl)nc(Cl)nc23)O1)OC(=O)C)OC(=O)C
Synonyms:
  • 2,6-Dichloro-9-(2,3,5-tri-O-acetyl-beta-D-ribofuranosyl)purine
  • 9-[2,3,5-Tri-O-Acetyl-Beta-D-Ribofuranosyl]-2,6-Dichloropurine
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