Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-β-D-glucopyranoside

≥98%

Reagent Code: #103989
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CAS Number 23661-28-1

science Other reagents with same CAS 23661-28-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 440.46 g/mol
Formula C₂₀H₂₄O₉S
badge Registry Numbers
MDL Number MFCD00135159
thermostat Physical Properties
Melting Point 116-120°C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates, this chemical plays a crucial role in carbohydrate chemistry. It is particularly valuable in the preparation of thioglycosides, which are essential for glycosylation reactions in the development of pharmaceuticals and biologically active compounds. Its acetyl-protected structure allows for selective deprotection, enabling precise modifications in the synthesis of oligosaccharides and glycoproteins. This makes it a key reagent in research focused on understanding carbohydrate-protein interactions and developing glycobiology-based therapeutics. Additionally, it is employed in the production of glycosidase inhibitors, which have potential applications in treating metabolic disorders and viral infections.

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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,480.00
inventory 5g
10-20 days ฿5,060.00
inventory 100mg
10-20 days ฿390.00
inventory 250mg
10-20 days ฿590.00

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Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-β-D-glucopyranoside
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Used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates, this chemical plays a crucial role in carbohydrate chemistry. It is particularly valuable in the preparation of thioglycosides, which are essential for glycosylation reactions in the development of pharmaceuticals and biologically active compounds. Its acetyl-protected structure allows for selective deprotection, enabling precise modifications in the synthesis of oligosaccharides and glycoproteins. This makes it a key

Used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates, this chemical plays a crucial role in carbohydrate chemistry. It is particularly valuable in the preparation of thioglycosides, which are essential for glycosylation reactions in the development of pharmaceuticals and biologically active compounds. Its acetyl-protected structure allows for selective deprotection, enabling precise modifications in the synthesis of oligosaccharides and glycoproteins. This makes it a key reagent in research focused on understanding carbohydrate-protein interactions and developing glycobiology-based therapeutics. Additionally, it is employed in the production of glycosidase inhibitors, which have potential applications in treating metabolic disorders and viral infections.

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