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

≥98%(GC)

Reagent Code: #103960
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CAS Number 13350-45-3

science Other reagents with same CAS 13350-45-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 378.39 g/mol
Formula C₁₅H₂₂O₉S
thermostat Physical Properties
Melting Point 91°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of thioglycosides, which are essential in glycosylation reactions. These reactions are fundamental in the production of oligosaccharides and glycoproteins, which have significant applications in biochemical research and pharmaceutical development. Additionally, it is used in the study of enzymatic processes and the development of glycosidase inhibitors, which are important in treating various metabolic disorders. Its acetylated form provides protection for reactive hydroxyl groups, ensuring selective reactivity in synthetic pathways.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Almost White Powder to Crystal
Purity (%) 98.0-100
Specific Rotation [A]20/D (C=1, CHCl3)(°) -17--13
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,340.00
Methyl 2,3,4,6-Tetra-O-acetyl-1-thio-β-D-glucopyranoside
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This chemical is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of thioglycosides, which are essential in glycosylation reactions. These reactions are fundamental in the production of oligosaccharides and glycoproteins, which have significant applications in biochemical research and pharmaceutical development. Additionally, it is used in the study of enzymatic processes and the development of glycosidase inhibitors, whi

This chemical is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of thioglycosides, which are essential in glycosylation reactions. These reactions are fundamental in the production of oligosaccharides and glycoproteins, which have significant applications in biochemical research and pharmaceutical development. Additionally, it is used in the study of enzymatic processes and the development of glycosidase inhibitors, which are important in treating various metabolic disorders. Its acetylated form provides protection for reactive hydroxyl groups, ensuring selective reactivity in synthetic pathways.

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