2-Azidoethyl 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranoside

≥92%

Reagent Code: #103687
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CAS Number 140428-81-5

science Other reagents with same CAS 140428-81-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 417.37 g/mol
Formula C₁₆H₂₃N₃O₁₀
inventory_2 Storage & Handling
Storage 2-8°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 glycosyl azides, which are valuable for click chemistry reactions, particularly the copper-catalyzed azide-alkyne cycloaddition (CuAAC). This reaction is widely employed in bioconjugation, labeling, and the development of bioactive molecules, including drug candidates and diagnostic probes. Additionally, its acetyl-protected glucose moiety makes it suitable for selective deprotection and further functionalization, enabling the creation of tailored carbohydrate structures for studying biological processes or designing glycotherapeutics.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to almost white powder or crystal
Purity (%) 91.5-100
Specific Rotation [A]20/D (C=1.5, CHCl3) -40.0 to -33.0
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,440.00
inventory 200mg
10-20 days ฿4,680.00

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2-Azidoethyl 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranoside
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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 glycosyl azides, which are valuable for click chemistry reactions, particularly the copper-catalyzed azide-alkyne cycloaddition (CuAAC). This reaction is widely employed in bioconjugation, labeling, and the development of bioactive molecules, including drug candidates and diagnostic probes. Addi

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 glycosyl azides, which are valuable for click chemistry reactions, particularly the copper-catalyzed azide-alkyne cycloaddition (CuAAC). This reaction is widely employed in bioconjugation, labeling, and the development of bioactive molecules, including drug candidates and diagnostic probes. Additionally, its acetyl-protected glucose moiety makes it suitable for selective deprotection and further functionalization, enabling the creation of tailored carbohydrate structures for studying biological processes or designing glycotherapeutics.

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