2,3,4,6-Tetra-O-benzyl-β-D-glucopyranosyl Fluoride

≥96%

Reagent Code: #103663
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CAS Number 78153-79-4

science Other reagents with same CAS 78153-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 542.65 g/mol
Formula C₃₄H₃₅FO₅
badge Registry Numbers
MDL Number MFCD01862264
thermostat Physical Properties
Melting Point 45-49°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in glycosylation reactions. It serves as a key intermediate for the construction of complex carbohydrate structures. Its benzyl groups provide protection for hydroxyl functionalities, allowing selective manipulation of the sugar moiety. The fluoride group acts as a leaving group, facilitating the formation of glycosidic bonds with various acceptors. This makes it valuable in the synthesis of oligosaccharides, glycoconjugates, and other biologically relevant molecules. It is also employed in the development of glycosidase inhibitors and in studies related to enzymatic glycosylation mechanisms. Its stability and reactivity make it a preferred choice in carbohydrate chemistry research and pharmaceutical applications.

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inventory 100mg
10-20 days ฿2,709.00

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2,3,4,6-Tetra-O-benzyl-β-D-glucopyranosyl Fluoride
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This compound is primarily utilized in organic synthesis, particularly in glycosylation reactions. It serves as a key intermediate for the construction of complex carbohydrate structures. Its benzyl groups provide protection for hydroxyl functionalities, allowing selective manipulation of the sugar moiety. The fluoride group acts as a leaving group, facilitating the formation of glycosidic bonds with various acceptors. This makes it valuable in the synthesis of oligosaccharides, glycoconjugates, and othe

This compound is primarily utilized in organic synthesis, particularly in glycosylation reactions. It serves as a key intermediate for the construction of complex carbohydrate structures. Its benzyl groups provide protection for hydroxyl functionalities, allowing selective manipulation of the sugar moiety. The fluoride group acts as a leaving group, facilitating the formation of glycosidic bonds with various acceptors. This makes it valuable in the synthesis of oligosaccharides, glycoconjugates, and other biologically relevant molecules. It is also employed in the development of glycosidase inhibitors and in studies related to enzymatic glycosylation mechanisms. Its stability and reactivity make it a preferred choice in carbohydrate chemistry research and pharmaceutical applications.

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