Methyl 2,3,4,6-tetra-O-benzyl-a-D-galactopyranoside

98%

Reagent Code: #103954
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CAS Number 53008-63-2

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scatter_plot Molecular Information
Weight 554.65 g/mol
Formula C₃₅H₃₈O₆
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MDL Number MFCD09756157
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosides and oligosaccharides, which are crucial in biochemical and pharmaceutical research. The compound is particularly valuable in the study of carbohydrate-protein interactions, aiding in the development of glycobiology-based therapeutics. Additionally, it is employed in the synthesis of glycosyl donors, which are essential for constructing specific glycosidic linkages in carbohydrate chemistry. Its benzyl-protected groups provide stability during synthetic processes, making it a versatile reagent in organic synthesis.

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inventory 1g
10-20 days ฿3,600.00

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Methyl 2,3,4,6-tetra-O-benzyl-a-D-galactopyranoside
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This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosides and oligosaccharides, which are crucial in biochemical and pharmaceutical research. The compound is particularly valuable in the study of carbohydrate-protein interactions, aiding in the development of glycobiology-based therapeutics. Additionally, it is employed in the synthesis of glycosyl donors, which are essential for constructing specific gl

This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosides and oligosaccharides, which are crucial in biochemical and pharmaceutical research. The compound is particularly valuable in the study of carbohydrate-protein interactions, aiding in the development of glycobiology-based therapeutics. Additionally, it is employed in the synthesis of glycosyl donors, which are essential for constructing specific glycosidic linkages in carbohydrate chemistry. Its benzyl-protected groups provide stability during synthetic processes, making it a versatile reagent in organic synthesis.

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