(2S,3R,4R,5S,6R)-3,4,5-Tris(benzyloxy)-2-methyl-6-(p-tolylthio)tetrahydro-2H-pyran

(2S,3R,4R,5S,6R)-3,4,5-Tris(benzyloxy)-2-methyl-6-(p-tolylthio)tetrahydro-2H-pyran

 Product Information

• CAS Number: 211801-54-6
• Catalog Number: A23-1063
• Molecular Formula: C₃₄H₃₈O₄S
• Molecular Weight: ~542.73 g/mol
• Purity: ≥ 98%

 Description

This compound is a protected thioglycoside derivative widely used as a glycosyl donor/intermediate in carbohydrate chemistry. The presence of benzyloxy protecting groups ensures stability during multi-step synthesis, while the p-tolylthio group enables activation under mild conditions for glycosylation reactions.

 Applications

• Glycosylation reactions in oligosaccharide synthesis
• Preparation of glycoconjugates and biologically active molecules
• Research in glycobiology and carbohydrate-based drug development
• Intermediate in stereoselective synthesis of complex sugars

Key Features

• High stereochemical purity
• Stable benzyl-protected structure
• Efficient thioglycoside activation
• Suitable for advanced synthetic protocols

 Storage

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