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

≥98%

Reagent Code: #103886
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CAS Number 41670-79-5

science Other reagents with same CAS 41670-79-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 392.42 g/mol
Formula C₁₆H₂₄O₉S
badge Registry Numbers
MDL Number MFCD00797608
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is a protected ethyl thioglycoside primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key glycosyl donor in glycosylation reactions. These reactions are crucial for constructing oligosaccharides and glycoproteins, which have significant applications in biochemistry and pharmaceutical research. Additionally, it is employed in the development of glycosidase inhibitors, which are potential therapeutic agents for treating diseases like diabetes and viral infections. Its acetyl-protected form ensures stability during chemical transformations, making it a valuable reagent in organic synthesis.

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Test Parameter Specification
Appearance White Crystals
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,860.00
inventory 1g
10-20 days ฿6,310.00

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Ethyl 2,3,4,6-Tetra-O-acetyl -1-thio-α-D-glucopyranoside
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This chemical is a protected ethyl thioglycoside primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key glycosyl donor in glycosylation reactions. These reactions are crucial for constructing oligosaccharides and glycoproteins, which have significant applications in biochemistry and pharmaceutical research. Additionally, it is employed in the development of glycosidase inhibitors, which are potential therapeutic agents for treating diseases like diabetes and vira

This chemical is a protected ethyl thioglycoside primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key glycosyl donor in glycosylation reactions. These reactions are crucial for constructing oligosaccharides and glycoproteins, which have significant applications in biochemistry and pharmaceutical research. Additionally, it is employed in the development of glycosidase inhibitors, which are potential therapeutic agents for treating diseases like diabetes and viral infections. Its acetyl-protected form ensures stability during chemical transformations, making it a valuable reagent in organic synthesis.

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