Ethyl 4,6-O-Benzylidene-3-O-(2-methylnaphthyl)-2-O-benzoyl-β-D-thioglucopyranoside

≥98%

Reagent Code: #103884
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CAS Number 352008-11-8

science Other reagents with same CAS 352008-11-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 486.09 g/mol
Formula C₃₃H₃₂O₆S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly in carbohydrate chemistry. It serves as a key intermediate in the preparation of complex glycosides and glycoconjugates. The benzylidene and benzoyl protecting groups make it valuable for selective deprotection strategies, enabling precise modifications to the sugar moiety. Additionally, its thioglucopyranoside structure is advantageous in the development of glycosidase inhibitors, which have potential applications in medicinal chemistry for treating diseases like diabetes and viral infections. Its stability and reactivity also make it suitable for use in the synthesis of glycosyl donors, which are essential in the construction of oligosaccharides and glycoproteins.

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Test Parameter Specification
Appearance White to off-white Solid
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿6,453.00
inventory 100mg
10-20 days ฿1,611.00
inventory 1g
10-20 days ฿11,322.00

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Ethyl 4,6-O-Benzylidene-3-O-(2-methylnaphthyl)-2-O-benzoyl-β-D-thioglucopyranoside
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This compound is primarily utilized in the field of organic synthesis, particularly in carbohydrate chemistry. It serves as a key intermediate in the preparation of complex glycosides and glycoconjugates. The benzylidene and benzoyl protecting groups make it valuable for selective deprotection strategies, enabling precise modifications to the sugar moiety. Additionally, its thioglucopyranoside structure is advantageous in the development of glycosidase inhibitors, which have potential applications in med

This compound is primarily utilized in the field of organic synthesis, particularly in carbohydrate chemistry. It serves as a key intermediate in the preparation of complex glycosides and glycoconjugates. The benzylidene and benzoyl protecting groups make it valuable for selective deprotection strategies, enabling precise modifications to the sugar moiety. Additionally, its thioglucopyranoside structure is advantageous in the development of glycosidase inhibitors, which have potential applications in medicinal chemistry for treating diseases like diabetes and viral infections. Its stability and reactivity also make it suitable for use in the synthesis of glycosyl donors, which are essential in the construction of oligosaccharides and glycoproteins.

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