4-Methylphenyl 4,6-O-Benzylidene-2,3-di-O-benzoyl-1-thio-β-D-glucopyranoside

≥98%

Reagent Code: #103729
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CAS Number 323195-40-0

science Other reagents with same CAS 323195-40-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 582.17 g/mol
Formula C₃₄H₃₀O₇S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily used in organic synthesis and carbohydrate chemistry as a protected glycosyl donor. Its structure, featuring benzylidene and benzoyl protecting groups, makes it a valuable intermediate for the selective formation of glycosidic bonds. It is particularly useful in the synthesis of complex oligosaccharides and glycoconjugates, which are essential in the development of pharmaceuticals and bioactive molecules. The thio-glycoside moiety enhances its stability and reactivity, allowing for controlled glycosylation reactions. Additionally, it finds applications in the study of enzymatic processes and the development of glycosidase inhibitors, which are relevant in treating diseases like diabetes and viral infections.

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Test Parameter Specification
Appearance White Powder
Purity (%) 98-100%
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿3,190.00
inventory 100mg
10-20 days ฿1,130.00
inventory 1g
10-20 days ฿5,140.00

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4-Methylphenyl 4,6-O-Benzylidene-2,3-di-O-benzoyl-1-thio-β-D-glucopyranoside
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This compound is primarily used in organic synthesis and carbohydrate chemistry as a protected glycosyl donor. Its structure, featuring benzylidene and benzoyl protecting groups, makes it a valuable intermediate for the selective formation of glycosidic bonds. It is particularly useful in the synthesis of complex oligosaccharides and glycoconjugates, which are essential in the development of pharmaceuticals and bioactive molecules. The thio-glycoside moiety enhances its stability and reactivity, allowing

This compound is primarily used in organic synthesis and carbohydrate chemistry as a protected glycosyl donor. Its structure, featuring benzylidene and benzoyl protecting groups, makes it a valuable intermediate for the selective formation of glycosidic bonds. It is particularly useful in the synthesis of complex oligosaccharides and glycoconjugates, which are essential in the development of pharmaceuticals and bioactive molecules. The thio-glycoside moiety enhances its stability and reactivity, allowing for controlled glycosylation reactions. Additionally, it finds applications in the study of enzymatic processes and the development of glycosidase inhibitors, which are relevant in treating diseases like diabetes and viral infections.

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