1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-glucopyranose

≥98%

Reagent Code: #103620
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CAS Number 56883-33-1

science Other reagents with same CAS 56883-33-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.32 g/mol
Formula C₁₄H₁₉N₃O₉
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is widely used in carbohydrate chemistry and glycobiology research as a key intermediate for synthesizing complex glycoconjugates. Its azido group allows for selective chemical modifications through click chemistry, particularly in the preparation of glycosyl donors or acceptors. It is instrumental in the synthesis of oligosaccharides, glycopeptides, and glycoproteins, which are essential for studying biological processes like cell signaling and immune responses. Additionally, it serves as a precursor for creating glycosaminoglycan analogs, which are important in drug development and tissue engineering. Its acetyl groups provide protection during synthetic steps, ensuring selective reactivity in multi-step organic transformations.

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Test Parameter Specification
Appearance White Powder
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿49,880.00
inventory 250mg
10-20 days ฿5,800.00
inventory 1g
10-20 days ฿12,870.00
inventory 100mg
10-20 days ฿2,980.00

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1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-glucopyranose
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This compound is widely used in carbohydrate chemistry and glycobiology research as a key intermediate for synthesizing complex glycoconjugates. Its azido group allows for selective chemical modifications through click chemistry, particularly in the preparation of glycosyl donors or acceptors. It is instrumental in the synthesis of oligosaccharides, glycopeptides, and glycoproteins, which are essential for studying biological processes like cell signaling and immune responses. Additionally, it serves as

This compound is widely used in carbohydrate chemistry and glycobiology research as a key intermediate for synthesizing complex glycoconjugates. Its azido group allows for selective chemical modifications through click chemistry, particularly in the preparation of glycosyl donors or acceptors. It is instrumental in the synthesis of oligosaccharides, glycopeptides, and glycoproteins, which are essential for studying biological processes like cell signaling and immune responses. Additionally, it serves as a precursor for creating glycosaminoglycan analogs, which are important in drug development and tissue engineering. Its acetyl groups provide protection during synthetic steps, ensuring selective reactivity in multi-step organic transformations.

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