2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl Azide

≥98%

Reagent Code: #103652
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CAS Number 53784-29-5

science Other reagents with same CAS 53784-29-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.32 g/mol
Formula C₁₄H₁₉N₃O₉
badge Registry Numbers
MDL Number MFCD05664724
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycosides and glycoconjugates. It serves as a versatile building block in click chemistry reactions, particularly in copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole-linked glycoconjugates. These glycoconjugates are valuable in drug discovery, bioconjugation, and the development of glycopeptides or glycoproteins. Additionally, it is employed in the synthesis of mannose-containing oligosaccharides, which are essential for studying carbohydrate-protein interactions and developing carbohydrate-based vaccines or therapeutics. Its acetylated form provides stability and controlled reactivity, making it suitable for selective glycosylation processes.

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Test Parameter Specification
Appearance Colorless to white to yellow solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,050.00
inventory 250mg
10-20 days ฿8,230.00

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2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl Azide
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This chemical is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycosides and glycoconjugates. It serves as a versatile building block in click chemistry reactions, particularly in copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole-linked glycoconjugates. These glycoconjugates are valuable in drug discovery, bioconjugation, and the development of glycopeptides or glycoproteins. Additionally, it is employed in the synthesis of mannose-containing oligosaccharides, which are essential for studying carbohydrate-protein interactions and developing carbohydrate-based vaccines or therapeutics. Its acetylated form provides stability and controlled reactivity, making it suitable for selective glycosylation processes.
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