3,4,6-Tri-O-benzyl-2-deoxy-D-galactopyranose

≥98%

Reagent Code: #103697
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CAS Number 94189-64-7

science Other reagents with same CAS 94189-64-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 434.53 g/mol
Formula C₂₇H₃₀O₅
badge Registry Numbers
MDL Number MFCD06797169
thermostat Physical Properties
Melting Point 83-87°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical 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 glycosides, oligosaccharides, and other biologically active molecules. Its benzyl-protected groups make it highly versatile for selective deprotection and further functionalization, enabling precise control over the structure of the final product. It is often employed in the development of pharmaceuticals, especially in the creation of glycosylated drugs and vaccines, where specific sugar moieties are crucial for biological activity. Additionally, it finds applications in research related to carbohydrate chemistry, aiding in the study of glycan structures and their interactions with proteins or other biomolecules.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿1,647.00

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3,4,6-Tri-O-benzyl-2-deoxy-D-galactopyranose
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This chemical 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 glycosides, oligosaccharides, and other biologically active molecules. Its benzyl-protected groups make it highly versatile for selective deprotection and further functionalization, enabling precise control over the structure of the final product. It is often employed in the development of pharmaceuticals, especially in the

This chemical 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 glycosides, oligosaccharides, and other biologically active molecules. Its benzyl-protected groups make it highly versatile for selective deprotection and further functionalization, enabling precise control over the structure of the final product. It is often employed in the development of pharmaceuticals, especially in the creation of glycosylated drugs and vaccines, where specific sugar moieties are crucial for biological activity. Additionally, it finds applications in research related to carbohydrate chemistry, aiding in the study of glycan structures and their interactions with proteins or other biomolecules.

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