1,3,4,6-Tetra-O-acetyl-2-deoxy-2-[(2-azidoacetyl)amino]-β-D-glucopyranose

≥98%

Reagent Code: #103624
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CAS Number 98924-81-3

science Other reagents with same CAS 98924-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 430.37 g/mol
Formula C₁₆H₂₂N₄O₁₀
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily used in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex glycoconjugates, such as glycoproteins and glycolipids, due to its azido and acetyl protecting groups. The azido group allows for efficient click chemistry reactions, enabling the attachment of various functional groups or biomolecules. It is also employed in the preparation of glycosyl donors for oligosaccharide synthesis, facilitating the study of glycosylation processes and the development of carbohydrate-based therapeutics. Additionally, it finds application in the design of carbohydrate-based vaccines and drug delivery systems, leveraging its structural properties for targeted biological interactions.

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Test Parameter Specification
Appearance White Powder
Purity (%) 98-100%
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿10,380.00
inventory 100mg
10-20 days ฿34,600.00
inventory 5mg
10-20 days ฿3,480.00

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1,3,4,6-Tetra-O-acetyl-2-deoxy-2-[(2-azidoacetyl)amino]-β-D-glucopyranose
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This compound is primarily used in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex glycoconjugates, such as glycoproteins and glycolipids, due to its azido and acetyl protecting groups. The azido group allows for efficient click chemistry reactions, enabling the attachment of various functional groups or biomolecules. It is also employed in the preparation of glycosyl donors for oligosaccharide synthesis, facilitating the study of glycosylatio

This compound is primarily used in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex glycoconjugates, such as glycoproteins and glycolipids, due to its azido and acetyl protecting groups. The azido group allows for efficient click chemistry reactions, enabling the attachment of various functional groups or biomolecules. It is also employed in the preparation of glycosyl donors for oligosaccharide synthesis, facilitating the study of glycosylation processes and the development of carbohydrate-based therapeutics. Additionally, it finds application in the design of carbohydrate-based vaccines and drug delivery systems, leveraging its structural properties for targeted biological interactions.

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