1,3,4,6-Tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose

≥97%

Reagent Code: #103623
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CAS Number 10022-13-6

science Other reagents with same CAS 10022-13-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 477.42 g/mol
Formula C₂₂H₂₃NO₁₁
thermostat Physical Properties
Melting Point 200°C(lit.)
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is primarily used in the synthesis of complex carbohydrates and glycoconjugates, serving as a key intermediate in the preparation of biologically active molecules. It plays a significant role in glycosylation reactions, where it acts as a protected glycosyl donor, enabling the selective formation of glycosidic bonds. Its acetyl and phthalimido groups provide stability and control during chemical transformations, making it valuable in the production of oligosaccharides and glycoproteins. Additionally, it is utilized in research focused on developing new therapeutic agents, particularly in the field of glycobiology, where understanding carbohydrate interactions is crucial for drug design and vaccine development.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to almost white powder to crystal
Purity (%) 96.5-100%
Specific Rotation [α]20/D (C=1, CHCl3) 66-70
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,250.00
inventory 5g
10-20 days ฿5,180.00

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1,3,4,6-Tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose
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This compound is primarily used in the synthesis of complex carbohydrates and glycoconjugates, serving as a key intermediate in the preparation of biologically active molecules. It plays a significant role in glycosylation reactions, where it acts as a protected glycosyl donor, enabling the selective formation of glycosidic bonds. Its acetyl and phthalimido groups provide stability and control during chemical transformations, making it valuable in the production of oligosaccharides and glycoproteins. Add

This compound is primarily used in the synthesis of complex carbohydrates and glycoconjugates, serving as a key intermediate in the preparation of biologically active molecules. It plays a significant role in glycosylation reactions, where it acts as a protected glycosyl donor, enabling the selective formation of glycosidic bonds. Its acetyl and phthalimido groups provide stability and control during chemical transformations, making it valuable in the production of oligosaccharides and glycoproteins. Additionally, it is utilized in research focused on developing new therapeutic agents, particularly in the field of glycobiology, where understanding carbohydrate interactions is crucial for drug design and vaccine development.

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