(3-((((9H-Fluoren-9-yl)methoxy)carbonyl)oxy)-5-(benzyloxy)-6-(ethylthio)-4-(naphthalen-2-ylmethoxy)tetrahydro-2H-pyran-2-yl)methyl 4-oxopentanoate

(3-((((9H-Fluoren-9-yl)methoxy)carbonyl)oxy)-5-(benzyloxy)-6-(ethylthio)-4-(naphthalen-2-ylmethoxy)tetrahydro-2H-pyran-2-yl)methyl 4-oxopentanoate

Product Information

• CAS Number: Not Available
• Catalog Number: A23-1065
• Molecular Formula: C₄₂H₄₃NO₉S
• Molecular Weight: ~745.86 g/mol
• Purity: ≥ 98%

Description

This compound is a multi-protected thioglycoside derivative incorporating Fmoc, benzyl, and naphthylmethyl protecting groups, designed for advanced carbohydrate synthesis. The ethylthio functionality at the anomeric position allows controlled activation in glycosylation reactions, while the diverse protecting groups enable orthogonal deprotection strategies in complex synthetic workflows.

The presence of a 4-oxopentanoate linker further enhances its applicability in glycoconjugate and linker-based synthesis.

Applications

• Oligosaccharide and glycoconjugate synthesis
• Glycopeptide and linker-based molecular design
• Advanced carbohydrate chemistry research
• Development of biologically active glyco-derivatives

Key Features

• Orthogonal protection (Fmoc, benzyl, naphthylmethyl)
• Reactive thioglycoside donor (ethylthio group)
• High stereochemical integrity
• Suitable for multi-step synthesis and linker chemistry

Storage

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

Safety Information

• For research use only
• Use appropriate PPE (gloves, lab coat, eye protection)
• Handle under controlled laboratory conditions