Phenyl 4-O-acetyl-2,6-di-O-benzoyl-1-thio-β-thio-β-D-galactopyranoside

≥98%

Reagent Code: #96954
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CAS Number 152488-28-3

science Other reagents with same CAS 152488-28-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 522.57 g/mol
Formula C₂₈H₂₆O₈S
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycosides and glycoconjugates. Its structure, featuring protective groups like acetyl and benzoyl, makes it valuable for selective glycosylation reactions, enabling the construction of specific glycosidic bonds. It is particularly useful in the synthesis of oligosaccharides and glycoproteins, which are essential in biological studies and drug development. Additionally, it serves as a building block in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes and viral infections. Its thio-glycoside moiety enhances its reactivity, making it a versatile tool in synthetic organic chemistry.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿17,415.00
inventory 100mg
10-20 days ฿55,611.00
inventory 5mg
10-20 days ฿4,995.00

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Phenyl 4-O-acetyl-2,6-di-O-benzoyl-1-thio-β-thio-β-D-galactopyranoside
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This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycosides and glycoconjugates. Its structure, featuring protective groups like acetyl and benzoyl, makes it valuable for selective glycosylation reactions, enabling the construction of specific glycosidic bonds. It is particularly useful in the synthesis of oligosaccharides and glycoproteins, which are essential in biological studies and drug development. Additionally, it

This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycosides and glycoconjugates. Its structure, featuring protective groups like acetyl and benzoyl, makes it valuable for selective glycosylation reactions, enabling the construction of specific glycosidic bonds. It is particularly useful in the synthesis of oligosaccharides and glycoproteins, which are essential in biological studies and drug development. Additionally, it serves as a building block in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes and viral infections. Its thio-glycoside moiety enhances its reactivity, making it a versatile tool in synthetic organic chemistry.

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