4-Methoxyphenyl 3-O-Allyl-2-O-benzyl-4,6-O-benzylidene-β-D-galactopyranoside

98%

Reagent Code: #103735
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CAS Number 2160551-35-7

science Other reagents with same CAS 2160551-35-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 504.58 g/mol
Formula C₃₀H₃₂O₇
badge Registry Numbers
MDL Number MFCD06797140
thermostat Physical Properties
Melting Point 177℃
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is primarily used in organic synthesis and carbohydrate chemistry research. It serves as a key intermediate in the preparation of complex oligosaccharides and glycoconjugates. Its structure, featuring protective groups like benzyl and benzylidene, allows for selective manipulation during glycosylation reactions, making it valuable for constructing specific glycosidic linkages. Additionally, it is employed in studies focused on understanding enzymatic processes and developing glycosidase inhibitors, which have potential applications in drug discovery and therapeutic development. Its role in synthesizing bioactive molecules also extends to the field of glycobiology, where it aids in exploring cell-surface interactions and carbohydrate-based signaling pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,280.00

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4-Methoxyphenyl 3-O-Allyl-2-O-benzyl-4,6-O-benzylidene-β-D-galactopyranoside
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This chemical is primarily used in organic synthesis and carbohydrate chemistry research. It serves as a key intermediate in the preparation of complex oligosaccharides and glycoconjugates. Its structure, featuring protective groups like benzyl and benzylidene, allows for selective manipulation during glycosylation reactions, making it valuable for constructing specific glycosidic linkages. Additionally, it is employed in studies focused on understanding enzymatic processes and developing glycosidase inh

This chemical is primarily used in organic synthesis and carbohydrate chemistry research. It serves as a key intermediate in the preparation of complex oligosaccharides and glycoconjugates. Its structure, featuring protective groups like benzyl and benzylidene, allows for selective manipulation during glycosylation reactions, making it valuable for constructing specific glycosidic linkages. Additionally, it is employed in studies focused on understanding enzymatic processes and developing glycosidase inhibitors, which have potential applications in drug discovery and therapeutic development. Its role in synthesizing bioactive molecules also extends to the field of glycobiology, where it aids in exploring cell-surface interactions and carbohydrate-based signaling pathways.

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