2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl Azide

≥98%

Reagent Code: #116048
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CAS Number 6205-69-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.33 g/mol
Formula C₁₄H₂₀N₄O₈
badge Registry Numbers
MDL Number MFCD00216968
thermostat Physical Properties
Melting Point 167°C(dec.)(lit.)
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates, which are essential in biochemical and pharmaceutical research. It serves as a key intermediate in the preparation of glycosylamines and glycosyl azides, which are further utilized in click chemistry reactions. These reactions are crucial for developing bioconjugates, drug delivery systems, and labeling biomolecules. Additionally, it plays a role in the study of carbohydrate-protein interactions, aiding in the development of vaccines, diagnostics, and therapeutic agents targeting glycans. Its acetylated form provides stability and reactivity, making it a valuable building block in organic synthesis.

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Test Parameter Specification
Appearance White to light yellow to light orange powder to crystal
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days $203.43
inventory 200mg
10-20 days $57.95
2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl Azide
This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates, which are essential in biochemical and pharmaceutical research. It serves as a key intermediate in the preparation of glycosylamines and glycosyl azides, which are further utilized in click chemistry reactions. These reactions are crucial for developing bioconjugates, drug delivery systems, and labeling biomolecules. Additionally, it plays a role in the study of carbohydrate-protein interactions, aiding in the development of vaccines, diagnostics, and therapeutic agents targeting glycans. Its acetylated form provides stability and reactivity, making it a valuable building block in organic synthesis.
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