2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl Azide
≥98%
Reagent
Code: #116048
CAS Number
6205-69-2
blur_circular Chemical Specifications
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Molecular Information
Weight
372.33 g/mol
Formula
C₁₄H₂₀N₄O₈
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Registry Numbers
MDL Number
MFCD00216968
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Physical Properties
Melting Point
167°C(dec.)(lit.)
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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.
format_list_bulleted Product Specification
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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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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