3,4,6-Tri-O-acetyl-2-azido-2-deoxy-D-galactopyranoside

≥96%

Reagent Code: #103699
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CAS Number 83025-10-9

science Other reagents with same CAS 83025-10-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.27868 g/mol
Formula C₁₂H₁₇N₃O₈
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily used 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 biologically active molecules, particularly in the development of glycoproteins and glycolipids. Its azido group allows for selective chemical modifications, making it valuable in click chemistry applications. Additionally, it is utilized in the study of carbohydrate-protein interactions, aiding in the understanding of cellular processes and the development of therapeutic agents. Its acetylated form enhances stability and solubility, facilitating its use in organic synthesis and medicinal chemistry research.

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Test Parameter Specification
Appearance Off-White Solid
Purity (%) 95.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,680.00
inventory 100mg
10-20 days ฿6,380.00
inventory 1g
10-20 days ฿42,980.00

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3,4,6-Tri-O-acetyl-2-azido-2-deoxy-D-galactopyranoside
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This compound is primarily used 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 biologically active molecules, particularly in the development of glycoproteins and glycolipids. Its azido group allows for selective chemical modifications, making it valuable in click chemistry applications. Additionally, it is utilized in the study of carbohydrate-protein interactions, aiding in the under

This compound is primarily used 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 biologically active molecules, particularly in the development of glycoproteins and glycolipids. Its azido group allows for selective chemical modifications, making it valuable in click chemistry applications. Additionally, it is utilized in the study of carbohydrate-protein interactions, aiding in the understanding of cellular processes and the development of therapeutic agents. Its acetylated form enhances stability and solubility, facilitating its use in organic synthesis and medicinal chemistry research.

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