6-O-Acetyl-2,3,4-tri-O-benzyl-D-glucopyranose

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Reagent Code: #103761
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CAS Number 85011-34-3

science Other reagents with same CAS 85011-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 492.57 g/mol
Formula C₂₉H₃₂O₇
thermostat Physical Properties
Melting Point 100°C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of oligosaccharides, which are essential for studying biological processes such as cell signaling and immune response. The benzyl groups provide protection for hydroxyl groups during chemical reactions, allowing selective modifications to the sugar molecule. This selective protection is crucial in the stepwise construction of glycosidic bonds, which are fundamental in carbohydrate chemistry. Additionally, it is employed in the development of glycosylated natural products and pharmaceuticals, where precise control over sugar attachment is required. Its role in advancing glycobiology research makes it a valuable tool for understanding and manipulating carbohydrate-related biological functions.

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inventory 1g
10-20 days ฿7,600.00

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6-O-Acetyl-2,3,4-tri-O-benzyl-D-glucopyranose
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This compound is primarily used in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of oligosaccharides, which are essential for studying biological processes such as cell signaling and immune response. The benzyl groups provide protection for hydroxyl groups during chemical reactions, allowing selective modifications to the sugar molecule. This selective protection is crucial in the stepwise construction of

This compound is primarily used in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of oligosaccharides, which are essential for studying biological processes such as cell signaling and immune response. The benzyl groups provide protection for hydroxyl groups during chemical reactions, allowing selective modifications to the sugar molecule. This selective protection is crucial in the stepwise construction of glycosidic bonds, which are fundamental in carbohydrate chemistry. Additionally, it is employed in the development of glycosylated natural products and pharmaceuticals, where precise control over sugar attachment is required. Its role in advancing glycobiology research makes it a valuable tool for understanding and manipulating carbohydrate-related biological functions.

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