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CAS 171721-00-9

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1,3,5-Tri-O-benzoyl-2-deoxy-2-fluoro-alpha-L-arabinofuranose

Description:
1,3,5-Tri-O-benzoyl-2-deoxy-2-fluoro-alpha-L-arabinofuranose is a modified sugar derivative characterized by the presence of three benzoyl groups attached to the hydroxyl positions at the 1, 3, and 5 positions of the arabinofuranose ring. The substitution of a fluorine atom at the 2-position enhances its chemical stability and alters its reactivity compared to the parent sugar. This compound is typically used in organic synthesis and carbohydrate chemistry, particularly in the development of nucleoside analogs and other biologically active molecules. Its structure contributes to its potential applications in medicinal chemistry, where modifications to sugar moieties can influence biological activity and pharmacokinetics. The presence of the benzoyl groups also provides a means for further functionalization, making it a versatile intermediate in synthetic pathways. Overall, this compound exemplifies the intricate relationship between structure and function in carbohydrate chemistry, highlighting the importance of modifications in tailoring properties for specific applications.
Formula:C26H21FO7
InChI:InChI=1/C26H21FO7/c27-21-22(33-24(29)18-12-6-2-7-13-18)20(16-31-23(28)17-10-4-1-5-11-17)32-26(21)34-25(30)19-14-8-3-9-15-19/h1-15,20-22,26H,16H2/t20-,21+,22-,26-/m0/s1
Synonyms:
  • 2-Deoxy-2-Fluoro-1,3,5-Tri-O-Benzoyl-L-Ribofuranose
  • 2-Deoxy-2-Fluoro-1,3,5-Tri-O-Bza-L-Ribofuranose
  • 1,3,5-Tri-O-benzoyl-2-deoxy-2-fluoro-a-L-arabinofuranose
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