1-S-Ethyl 2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside

98%

Reagent Code: #103878
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CAS Number 125411-99-6

science Other reagents with same CAS 125411-99-6

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Weight 584.7648 g/mol
Formula C₃₆H₄₀O₅S
badge Registry Numbers
MDL Number MFCD13182895
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily used in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates. The benzyl protecting groups on the hydroxyl moieties make it a versatile building block for selective glycosylation reactions, enabling the construction of specific glycosidic linkages. Its thiogalactoside structure is particularly useful in enzymatic studies and the development of glycosidase inhibitors. Additionally, it finds applications in the preparation of glycoproteins and glycolipids, which are essential for studying cell-surface interactions and biological recognition processes. Its role in the synthesis of biologically active molecules makes it valuable in drug discovery and development.

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inventory 1g
10-20 days ฿12,230.00

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1-S-Ethyl 2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside
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This compound is primarily used in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates. The benzyl protecting groups on the hydroxyl moieties make it a versatile building block for selective glycosylation reactions, enabling the construction of specific glycosidic linkages. Its thiogalactoside structure is particularly useful in enzymatic studies and the development of glycosidase inhibitors. Additionally, it f

This compound is primarily used in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates. The benzyl protecting groups on the hydroxyl moieties make it a versatile building block for selective glycosylation reactions, enabling the construction of specific glycosidic linkages. Its thiogalactoside structure is particularly useful in enzymatic studies and the development of glycosidase inhibitors. Additionally, it finds applications in the preparation of glycoproteins and glycolipids, which are essential for studying cell-surface interactions and biological recognition processes. Its role in the synthesis of biologically active molecules makes it valuable in drug discovery and development.

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