Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

95%

Reagent Code: #103949
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CAS Number 63064-49-3

science Other reagents with same CAS 63064-49-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 349.38 g/mol
Formula C₁₈H₂₃NO₆
badge Registry Numbers
MDL Number MFCD15144921
thermostat Physical Properties
Melting Point 235-244 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis and carbohydrate chemistry research. It serves as a key intermediate in the preparation of complex glycosides and glycoconjugates, which are essential in studying biological processes and developing therapeutic agents. Its benzylidene protecting group allows selective modification of the carbohydrate structure, making it valuable in the synthesis of oligosaccharides and glycopeptides. Additionally, it is employed in the development of glycosidase inhibitors, which have potential applications in treating metabolic disorders and viral infections. Its role in advancing glycobiology and medicinal chemistry underscores its importance in scientific research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,172.00

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Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside
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This chemical is primarily utilized in organic synthesis and carbohydrate chemistry research. It serves as a key intermediate in the preparation of complex glycosides and glycoconjugates, which are essential in studying biological processes and developing therapeutic agents. Its benzylidene protecting group allows selective modification of the carbohydrate structure, making it valuable in the synthesis of oligosaccharides and glycopeptides. Additionally, it is employed in the development of glycosidase i

This chemical is primarily utilized in organic synthesis and carbohydrate chemistry research. It serves as a key intermediate in the preparation of complex glycosides and glycoconjugates, which are essential in studying biological processes and developing therapeutic agents. Its benzylidene protecting group allows selective modification of the carbohydrate structure, making it valuable in the synthesis of oligosaccharides and glycopeptides. Additionally, it is employed in the development of glycosidase inhibitors, which have potential applications in treating metabolic disorders and viral infections. Its role in advancing glycobiology and medicinal chemistry underscores its importance in scientific research.

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