3,4,6-tri-O-benzyl-D-glucofuranose

BR

Reagent Code: #103705
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CAS Number 35958-64-6

science Other reagents with same CAS 35958-64-6

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Weight 451.53144 g/mol
Formula C₂₇H₃₁O₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used extensively in organic synthesis as a protected intermediate for the preparation of complex carbohydrates and glycoconjugates. It plays a crucial role in the synthesis of oligosaccharides, where the benzyl groups act as protecting agents for hydroxyl groups, allowing selective deprotection and further functionalization. This compound is particularly valuable in the development of glycosylation strategies, enabling the creation of specific glycosidic bonds essential for producing biologically active molecules. Its application extends to the pharmaceutical industry, where it aids in the synthesis of carbohydrate-based drugs, vaccines, and diagnostic agents. Additionally, it is utilized in research to study carbohydrate metabolism and enzyme mechanisms, contributing to advancements in biochemistry and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿6,270.00

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3,4,6-tri-O-benzyl-D-glucofuranose
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Used extensively in organic synthesis as a protected intermediate for the preparation of complex carbohydrates and glycoconjugates. It plays a crucial role in the synthesis of oligosaccharides, where the benzyl groups act as protecting agents for hydroxyl groups, allowing selective deprotection and further functionalization. This compound is particularly valuable in the development of glycosylation strategies, enabling the creation of specific glycosidic bonds essential for producing biologically active

Used extensively in organic synthesis as a protected intermediate for the preparation of complex carbohydrates and glycoconjugates. It plays a crucial role in the synthesis of oligosaccharides, where the benzyl groups act as protecting agents for hydroxyl groups, allowing selective deprotection and further functionalization. This compound is particularly valuable in the development of glycosylation strategies, enabling the creation of specific glycosidic bonds essential for producing biologically active molecules. Its application extends to the pharmaceutical industry, where it aids in the synthesis of carbohydrate-based drugs, vaccines, and diagnostic agents. Additionally, it is utilized in research to study carbohydrate metabolism and enzyme mechanisms, contributing to advancements in biochemistry and medicinal chemistry.

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