Benzyl-6-[(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-galactopyranosyl)oxy]hexylcarbamat

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Reagent Code: #71246
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CAS Number 159173-77-0

science Other reagents with same CAS 159173-77-0

blur_circular Chemical Specifications

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Weight 580.62 g/mol
Formula C₂₈H₄₀N₂O₁₁
badge Registry Numbers
MDL Number MFCD30489047
inventory_2 Storage & Handling
Storage -20°C, store under inert gas

description Product Description

This compound is primarily utilized in the field of glycobiology and carbohydrate chemistry for the synthesis of complex glycoconjugates. It serves as a key intermediate in the preparation of glycopeptides and glycolipids, which are essential for studying cell-cell interactions, immune responses, and pathogen recognition mechanisms. Its acetylated sugar moiety allows for selective deprotection, enabling controlled glycosylation reactions. This chemical is also employed in the development of carbohydrate-based vaccines and therapeutics, particularly for targeting specific biological processes or diseases. Additionally, it is used in research to explore the role of glycosylation in protein function and stability, contributing to advancements in biotechnology and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,152.00
inventory 250mg
10-20 days ฿423.00
inventory 5g
10-20 days ฿4,041.00

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Benzyl-6-[(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-galactopyranosyl)oxy]hexylcarbamat
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This compound is primarily utilized in the field of glycobiology and carbohydrate chemistry for the synthesis of complex glycoconjugates. It serves as a key intermediate in the preparation of glycopeptides and glycolipids, which are essential for studying cell-cell interactions, immune responses, and pathogen recognition mechanisms. Its acetylated sugar moiety allows for selective deprotection, enabling controlled glycosylation reactions. This chemical is also employed in the development of carbohydrate-

This compound is primarily utilized in the field of glycobiology and carbohydrate chemistry for the synthesis of complex glycoconjugates. It serves as a key intermediate in the preparation of glycopeptides and glycolipids, which are essential for studying cell-cell interactions, immune responses, and pathogen recognition mechanisms. Its acetylated sugar moiety allows for selective deprotection, enabling controlled glycosylation reactions. This chemical is also employed in the development of carbohydrate-based vaccines and therapeutics, particularly for targeting specific biological processes or diseases. Additionally, it is used in research to explore the role of glycosylation in protein function and stability, contributing to advancements in biotechnology and medicinal chemistry.

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