1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-galactopyranose

≥98%

Reagent Code: #103618
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CAS Number 67817-30-5

science Other reagents with same CAS 67817-30-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.32 g/mol
Formula C₁₄H₁₉N₃O₉
badge Registry Numbers
MDL Number MFCD01076182
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a crucial role in glycosylation reactions. It serves as a key intermediate in the preparation of glycosyl donors, which are essential for constructing oligosaccharides and glycoproteins. Its azido group allows for further functionalization through click chemistry, enabling the attachment of various biomolecules or probes. This makes it valuable in glycobiology research, particularly in studying carbohydrate-protein interactions and developing glycoconjugate vaccines. Additionally, it is used in the production of modified sugars for drug development, where specific glycosylation patterns are required for therapeutic efficacy. Its acetyl groups provide stability during synthetic processes, ensuring efficient and selective reactions.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity (%) 97.5-100
Specific Rotation [A]20/D (C=1, CHCl3) 98-102
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿2,490.00

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1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-galactopyranose
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This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a crucial role in glycosylation reactions. It serves as a key intermediate in the preparation of glycosyl donors, which are essential for constructing oligosaccharides and glycoproteins. Its azido group allows for further functionalization through click chemistry, enabling the attachment of various biomolecules or probes. This makes it valuable in glycobiology research, particularly in studying carb

This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a crucial role in glycosylation reactions. It serves as a key intermediate in the preparation of glycosyl donors, which are essential for constructing oligosaccharides and glycoproteins. Its azido group allows for further functionalization through click chemistry, enabling the attachment of various biomolecules or probes. This makes it valuable in glycobiology research, particularly in studying carbohydrate-protein interactions and developing glycoconjugate vaccines. Additionally, it is used in the production of modified sugars for drug development, where specific glycosylation patterns are required for therapeutic efficacy. Its acetyl groups provide stability during synthetic processes, ensuring efficient and selective reactions.

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