2,3,4,6-Tetra-O-acetyl-D-mannopyranosyl Fluoride

>95.0%(GC)

Reagent Code: #103650
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CAS Number 174511-17-2

science Other reagents with same CAS 174511-17-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 350.30 g/mol
Formula C₁₄H₁₉FO₉
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in organic synthesis as a glycosyl donor for the preparation of complex carbohydrates and glycoconjugates. It is particularly valuable in the synthesis of oligosaccharides and glycoproteins, which are essential in biological and pharmaceutical research. The compound serves as a key intermediate in the development of glycosylation reactions, enabling the creation of specific glycosidic bonds. Its acetyl groups provide protection during synthetic processes, ensuring precise control over the final product's structure. This chemical is also employed in the study of enzyme mechanisms and carbohydrate-protein interactions, aiding in the design of novel therapeutic agents and biomaterials.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿34,119.00
inventory 1g
10-20 days ฿10,053.00

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2,3,4,6-Tetra-O-acetyl-D-mannopyranosyl Fluoride
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Used in organic synthesis as a glycosyl donor for the preparation of complex carbohydrates and glycoconjugates. It is particularly valuable in the synthesis of oligosaccharides and glycoproteins, which are essential in biological and pharmaceutical research. The compound serves as a key intermediate in the development of glycosylation reactions, enabling the creation of specific glycosidic bonds. Its acetyl groups provide protection during synthetic processes, ensuring precise control over the final prod

Used in organic synthesis as a glycosyl donor for the preparation of complex carbohydrates and glycoconjugates. It is particularly valuable in the synthesis of oligosaccharides and glycoproteins, which are essential in biological and pharmaceutical research. The compound serves as a key intermediate in the development of glycosylation reactions, enabling the creation of specific glycosidic bonds. Its acetyl groups provide protection during synthetic processes, ensuring precise control over the final product's structure. This chemical is also employed in the study of enzyme mechanisms and carbohydrate-protein interactions, aiding in the design of novel therapeutic agents and biomaterials.

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