4-O-Benzyl-D-glucal

98%

Reagent Code: #221168
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CAS Number 58871-11-7

science Other reagents with same CAS 58871-11-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.26 g/mol
Formula C₁₃H₁₆O₄
thermostat Physical Properties
Melting Point 99-103 °C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. Its main application lies in glycosylation reactions where selective formation of glycosidic bonds is required. The benzyl protecting group enhances stability and directs stereochemical outcomes during sugar coupling. It is widely employed in the development of pharmaceuticals, especially in the preparation of antiviral and anticancer agents that target cellular recognition processes involving carbohydrates. Also utilized in the construction of vaccine candidates and enzyme inhibitors due to its ability to mimic natural sugar structures.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿8,570.00
1g
10-20 days ฿28,590.00
4-O-Benzyl-D-glucal
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Used as a key intermediate in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. Its main application lies in glycosylation reactions where selective formation of glycosidic bonds is required. The benzyl protecting group enhances stability and directs stereochemical outcomes during sugar coupling. It is widely employed in the development of pharmaceuticals, especially in the preparation of antiviral and anticancer agents that target cellular recognition

Used as a key intermediate in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. Its main application lies in glycosylation reactions where selective formation of glycosidic bonds is required. The benzyl protecting group enhances stability and directs stereochemical outcomes during sugar coupling. It is widely employed in the development of pharmaceuticals, especially in the preparation of antiviral and anticancer agents that target cellular recognition processes involving carbohydrates. Also utilized in the construction of vaccine candidates and enzyme inhibitors due to its ability to mimic natural sugar structures.

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