4-Methoxyphenyl 2-Azido-4,6-O-benzylidene-2-deoxy-β-D-galactopyranoside

GR

Reagent Code: #103733
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CAS Number 1340541-47-0

science Other reagents with same CAS 1340541-47-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 399.4 g/mol
Formula C₂₀H₂₁N₃O₆
inventory_2 Storage & Handling
Storage 2-8℃, dry

description Product Description

This compound is primarily utilized in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates, which are essential for studying biological processes such as cell signaling and immune response. The azido group in the molecule allows for click chemistry applications, enabling efficient and selective conjugation with other biomolecules. Additionally, the benzylidene protecting group provides stability during synthetic transformations, ensuring precise control over the glycosylation process. Its application extends to the development of glycoprotein-based therapeutics and the exploration of carbohydrate-protein interactions in drug discovery.

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inventory 1mg
10-20 days ฿9,300.00

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4-Methoxyphenyl 2-Azido-4,6-O-benzylidene-2-deoxy-β-D-galactopyranoside
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This compound is primarily utilized in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates, which are essential for studying biological processes such as cell signaling and immune response. The azido group in the molecule allows for click chemistry applications, enabling efficient and selective conjugation with other biomolecules. Additionally, the benzylidene protecting group provides stability during syntheti

This compound is primarily utilized in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates, which are essential for studying biological processes such as cell signaling and immune response. The azido group in the molecule allows for click chemistry applications, enabling efficient and selective conjugation with other biomolecules. Additionally, the benzylidene protecting group provides stability during synthetic transformations, ensuring precise control over the glycosylation process. Its application extends to the development of glycoprotein-based therapeutics and the exploration of carbohydrate-protein interactions in drug discovery.

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