Ethyl 2,3,4,6-Tetra-O-acetyl-1-thio-β-D-glucopyranoside

≥99%

Reagent Code: #103879
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CAS Number 52645-73-5

science Other reagents with same CAS 52645-73-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 392.4214 g/mol
Formula C₁₆H₂₄O₉S
badge Registry Numbers
MDL Number MFCD04114310
thermostat Physical Properties
Melting Point 78-79℃
inventory_2 Storage & Handling
Density 1.27g/ml
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of glycosides. It serves as a protected form of thioglucose, enabling controlled glycosylation reactions. Its acetyl groups protect hydroxyl functionalities, allowing selective modifications in complex carbohydrate synthesis. It is particularly useful in the development of glycosyl donors for the synthesis of oligosaccharides, glycoconjugates, and other biologically active molecules. Its stability and reactivity make it a valuable tool in the study of enzymatic glycosylation processes and the production of glycostructures for pharmaceutical and biochemical research.

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Test Parameter Specification
Appearance White To Off-White Solid
Purity (%) 98.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿720.00
inventory 1g
10-20 days ฿1,780.00

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Ethyl 2,3,4,6-Tetra-O-acetyl-1-thio-β-D-glucopyranoside
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This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of glycosides. It serves as a protected form of thioglucose, enabling controlled glycosylation reactions. Its acetyl groups protect hydroxyl functionalities, allowing selective modifications in complex carbohydrate synthesis. It is particularly useful in the development of glycosyl donors for the synthesis of oligosaccharides, glycoconjugates, and other biologically active molecules.

This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of glycosides. It serves as a protected form of thioglucose, enabling controlled glycosylation reactions. Its acetyl groups protect hydroxyl functionalities, allowing selective modifications in complex carbohydrate synthesis. It is particularly useful in the development of glycosyl donors for the synthesis of oligosaccharides, glycoconjugates, and other biologically active molecules. Its stability and reactivity make it a valuable tool in the study of enzymatic glycosylation processes and the production of glycostructures for pharmaceutical and biochemical research.

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