Methyl 2,3,4-Tri-O-benzyl-1-thio-β-L-fucopyranoside

≥95%(HPLC)

Reagent Code: #103956
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CAS Number 107802-80-2

science Other reagents with same CAS 107802-80-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 464.62 g/mol
Formula C₂₈H₃₂O₄S
badge Registry Numbers
MDL Number MFCD06797141
thermostat Physical Properties
Melting Point 58°C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of fucose-containing oligosaccharides, which are important in biological processes such as cell-cell recognition and signaling. Its benzyl protecting groups make it a valuable building block for selective glycosylation reactions, enabling the construction of specific glycosidic linkages. Additionally, it is employed in the development of glycopeptides and glycoproteins, which have applications in drug discovery and the study of carbohydrate-protein interactions. Its stability and reactivity make it a preferred choice for researchers working on carbohydrate chemistry and glycobiology.

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inventory 250mg
10-20 days ฿6,651.00

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Methyl 2,3,4-Tri-O-benzyl-1-thio-β-L-fucopyranoside
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This chemical is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of fucose-containing oligosaccharides, which are important in biological processes such as cell-cell recognition and signaling. Its benzyl protecting groups make it a valuable building block for selective glycosylation reactions, enabling the construction of specific glycosidic linkages. Additionally, it is employed in the

This chemical is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of fucose-containing oligosaccharides, which are important in biological processes such as cell-cell recognition and signaling. Its benzyl protecting groups make it a valuable building block for selective glycosylation reactions, enabling the construction of specific glycosidic linkages. Additionally, it is employed in the development of glycopeptides and glycoproteins, which have applications in drug discovery and the study of carbohydrate-protein interactions. Its stability and reactivity make it a preferred choice for researchers working on carbohydrate chemistry and glycobiology.

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