1,3,5-Tri-O-benzoyl-alpha-d-ribofuranose

• CAT Number: L042282
• CAS Number: 22224-41-5
• Molecular Formula: C26H22O8
• Molecular Weight: 462.40
• Purity: ≥95%
• Target: Nucleoside Antimetabolite/Analog
• IUPAC Name: [(2R,3S,4R,5R)-3,5-dibenzoyloxy-4-hydroxyoxolan-2-yl]methyl benzoate
• InChI: InChI=1S/C26H22O8/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/h1-15,20-22,26-27H,16H2/t20-,21-,22-,26-/m1/s1
• InChIKey: HUHVPBKTTFVAQF-PIXQIBFHSA-N
• SMILES: C1=CC=C(C=C1)C(=O)OC[C@@H]2[C@H]([C@H]([C@H](O2)OC(=O)C3=CC=CC=C3)O)OC(=O)C4=CC=CC=C4

1,3,5-Tri-O-benzoyl-alpha-D-ribofuranose(Cat No.:L042282) is a derivative of alpha-D-ribofuranose with three benzoyl groups attached to its hydroxyl moieties. It holds significance in pharmaceutical and organic chemistry. The benzoyl groups serve as protecting groups, offering control in synthetic reactions, making them valuable in drug development and chemical synthesis. In pharmaceutical research, it may be used for the preparation of carbohydrate-based molecules with potential bioactive properties. Its adaptable structure may also find applications in material chemistry, potentially contributing to polymers, coatings, or surface modifications.