2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl chloride

98%

Reagent Code: #103942
label
Alias 2,3,4,6-tetra-O-acetyl-ALPHA-D-glucose chloride; ACETOCHLORO-ALPHA-D-GLUCOSE
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CAS Number 4451-35-8

science Other reagents with same CAS 4451-35-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 366.75 g/mol
Formula C₁₄H₁₉ClO₉
badge Registry Numbers
MDL Number MFCD00190701
thermostat Physical Properties
Melting Point 98-101℃ (ethyl ether )
inventory_2 Storage & Handling
Density 1.33±0.1 g/cm3 (20 ºC 760 Torr)
Storage 2-8℃, dry

description Product Description

This chemical is primarily used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates. It plays a key role in glycosylation reactions, where it acts as a glycosyl donor to form glycosidic bonds. This is particularly important in the production of oligosaccharides, polysaccharides, and glycoproteins, which have applications in biochemical research and pharmaceutical development. Additionally, it is utilized in the preparation of glycosylated natural products and in the study of enzymatic processes related to carbohydrate metabolism. Its acetylated form ensures stability and reactivity in synthetic procedures, making it a valuable reagent in organic and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,817.00

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2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl chloride
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This chemical is primarily used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates. It plays a key role in glycosylation reactions, where it acts as a glycosyl donor to form glycosidic bonds. This is particularly important in the production of oligosaccharides, polysaccharides, and glycoproteins, which have applications in biochemical research and pharmaceutical development. Additionally, it is utilized in the preparation of glycosylated natural products and in the study of

This chemical is primarily used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates. It plays a key role in glycosylation reactions, where it acts as a glycosyl donor to form glycosidic bonds. This is particularly important in the production of oligosaccharides, polysaccharides, and glycoproteins, which have applications in biochemical research and pharmaceutical development. Additionally, it is utilized in the preparation of glycosylated natural products and in the study of enzymatic processes related to carbohydrate metabolism. Its acetylated form ensures stability and reactivity in synthetic procedures, making it a valuable reagent in organic and medicinal chemistry.

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