(2S,3R,4R,5R,6R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)oxy)-5-(benzyloxy)-6-((benzyloxy)methyl)-2-(p-tolylthio)tetrahydro-2H-pyran-3-yl benzoate

(2S,3R,4R,5R,6R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)oxy)-5-(benzyloxy)-6-((benzyloxy)methyl)-2-(p-tolylthio)tetrahydro-2H-pyran-3-yl benzoate

Product Information

• CAS Number: Not  Available
• Catalog Number: A23-1067
• Molecular Formula: C₄₆H₄₅NO₈S
• Molecular Weight: ~771.92 g/mol
• Purity: ≥ 98%

Description

This compound is a highly functionalized thioglycoside derivative incorporating Fmoc protection, benzyl ether groups, and a benzoate functionality. It is designed as an advanced intermediate for carbohydrate synthesis and complex glycosylation strategies.

The p-tolylthio group at the anomeric position enables efficient activation under mild conditions, making it a reliable glycosyl donor. The combination of Fmoc and benzyl protecting groups allows orthogonal deprotection, while the benzoate ester provides additional functional versatility in multi-step synthesis.

Applications

• Oligosaccharide and glycoconjugate synthesis
• Glycosylation reactions using thioglycoside donors
• Advanced carbohydrate and glycochemistry research
• Development of biologically active glyco-derivatives

Key Features

• Orthogonally protected (Fmoc and benzyl groups)
• Reactive thioglycoside donor (p-tolylthio group)
• Benzoate functionality for synthetic flexibility
• High stereochemical integrity and purity

Storage

• Store at 2–8°C
• Keep in a dry, inert atmosphere
• Protect from moisture and light