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

≥98%

Reagent Code: #103991
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CAS Number 167612-35-3

science Other reagents with same CAS 167612-35-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 526.6900000000001 g/mol
Formula C₃₃H₃₄O₄S
thermostat Physical Properties
Melting Point 106-110°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex carbohydrates and glycoconjugates. It serves as a protected form of L-fucose, allowing for selective manipulation in glycosylation reactions. Its benzyl groups protect hydroxyl functionalities, ensuring specificity during chemical transformations. This makes it valuable in the synthesis of biologically active molecules, such as oligosaccharides, glycoproteins, and glycolipids, which are essential in studying cell-cell interactions, immune responses, and pathogen recognition. Additionally, it is employed in the development of glycoconjugate vaccines and therapeutic agents targeting carbohydrate-mediated processes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,250.00
inventory 200mg
10-20 days ฿5,000.00

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Phenyl 2,3,4-Tri-O-benzyl-1-thio-β-L-fucopyranoside
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This compound is primarily utilized in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex carbohydrates and glycoconjugates. It serves as a protected form of L-fucose, allowing for selective manipulation in glycosylation reactions. Its benzyl groups protect hydroxyl functionalities, ensuring specificity during chemical transformations. This makes it valuable in the synthesis of biologically active molecules, such as oligosaccharides, glycoproteins, and glyco

This compound is primarily utilized in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex carbohydrates and glycoconjugates. It serves as a protected form of L-fucose, allowing for selective manipulation in glycosylation reactions. Its benzyl groups protect hydroxyl functionalities, ensuring specificity during chemical transformations. This makes it valuable in the synthesis of biologically active molecules, such as oligosaccharides, glycoproteins, and glycolipids, which are essential in studying cell-cell interactions, immune responses, and pathogen recognition. Additionally, it is employed in the development of glycoconjugate vaccines and therapeutic agents targeting carbohydrate-mediated processes.

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