2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl Azide

≥98%

Reagent Code: #103655
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CAS Number 13992-26-2

science Other reagents with same CAS 13992-26-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.32 g/mol
Formula C₁₄H₁₉N₃O₉
badge Registry Numbers
MDL Number MFCD00181721
thermostat Physical Properties
Melting Point 96-99 ℃(lit.)
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in click chemistry reactions, particularly in the formation of glycosyl triazoles through azide-alkyne cycloaddition. Its acetylated groups protect the hydroxyl functionalities during chemical transformations, allowing for selective deprotection and further modification. It is also employed in the development of glycopeptides, glycolipids, and other biologically active molecules, making it valuable in glycobiology research and drug discovery. Additionally, it is utilized in the preparation of carbohydrate-based vaccines and diagnostic tools, contributing to advancements in immunology and medical diagnostics.

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Test Parameter Specification
Appearance White Powder
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,390.00
inventory 5g
10-20 days ฿46,800.00
inventory 1g
10-20 days ฿13,180.00

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2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl Azide
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This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in click chemistry reactions, particularly in the formation of glycosyl triazoles through azide-alkyne cycloaddition. Its acetylated groups protect the hydroxyl functionalities during chemical transformations, allowing for selective deprotection and further modification. It is also employed in the development of glycopeptides, glycolipids, and other biologically active molecules,

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in click chemistry reactions, particularly in the formation of glycosyl triazoles through azide-alkyne cycloaddition. Its acetylated groups protect the hydroxyl functionalities during chemical transformations, allowing for selective deprotection and further modification. It is also employed in the development of glycopeptides, glycolipids, and other biologically active molecules, making it valuable in glycobiology research and drug discovery. Additionally, it is utilized in the preparation of carbohydrate-based vaccines and diagnostic tools, contributing to advancements in immunology and medical diagnostics.

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