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CAS 159414-97-8

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N4-Acetyl-2'-Fluoro-2'-deoxycytidine

Description:
N4-Acetyl-2'-Fluoro-2'-deoxycytidine, commonly referred to as a modified nucleoside, is characterized by the presence of an acetyl group at the N4 position and a fluorine atom at the 2' position of the deoxycytidine structure. This modification enhances its stability and can influence its biological activity, particularly in the context of antiviral and anticancer research. The fluorine substitution can affect the nucleoside's interaction with enzymes and its incorporation into nucleic acids, potentially altering its pharmacokinetic properties. The compound is typically studied for its role in nucleic acid synthesis and as a potential therapeutic agent. Its molecular structure contributes to its unique properties, making it a subject of interest in medicinal chemistry and drug development. Additionally, the compound's CAS number, 159414-97-8, allows for precise identification in chemical databases and literature, facilitating research and application in various scientific fields.
Formula:C11H14FN3O5
InChI:InChI=1S/C11H14FN3O5/c1-5(17)13-7-2-3-15(11(19)14-7)10-8(12)9(18)6(4-16)20-10/h2-3,6,8-10,16,18H,4H2,1H3,(H,13,14,17,19)/t6-,8-,9-,10-/m1/s1
SMILES:CC(=Nc1ccn([C@H]2[C@@H]([C@@H]([C@@H](CO)O2)O)F)c(=O)n1)O
Synonyms:
  • N4-Acetyl-2'-Deoxy-2'-Fluorocytidine
  • N4-Ac-2'-F-dC
  • N-(1-((2R,3R,4R,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide
  • N4-Acetyl-2'-Fluoro-2'-deoxycytidine
  • Ac-2'-F-dC
  • N4-Acetyl-2'-Fluoro-2'-deoxycytidine USP/EP/BP
  • Cytidine, N-acetyl-2'-deoxy-2'-fluoro-
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