4-Methoxyphenyl 3-O-Benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

GR

Reagent Code: #103738
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CAS Number 138906-44-2

science Other reagents with same CAS 138906-44-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 505.52 g/mol
Formula C₂₈H₂₇NO₈
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is primarily used in organic synthesis and pharmaceutical research, particularly in the development of glycosides and carbohydrate-based compounds. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates, which are essential for studying biological processes such as cell signaling and immune responses. Additionally, it is employed in the preparation of glycosidase inhibitors and other bioactive molecules with potential therapeutic applications. Its benzyl and phthalimido protecting groups make it valuable in selective glycosylation reactions, enabling precise control over the structure of the final product.

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inventory 1mg
10-20 days ฿9,300.00

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4-Methoxyphenyl 3-O-Benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
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This chemical is primarily used in organic synthesis and pharmaceutical research, particularly in the development of glycosides and carbohydrate-based compounds. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates, which are essential for studying biological processes such as cell signaling and immune responses. Additionally, it is employed in the preparation of glycosidase inhibitors and other bioactive molecules with potential therapeutic applications. Its b

This chemical is primarily used in organic synthesis and pharmaceutical research, particularly in the development of glycosides and carbohydrate-based compounds. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates, which are essential for studying biological processes such as cell signaling and immune responses. Additionally, it is employed in the preparation of glycosidase inhibitors and other bioactive molecules with potential therapeutic applications. Its benzyl and phthalimido protecting groups make it valuable in selective glycosylation reactions, enabling precise control over the structure of the final product.

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