β-D-Gentiobiose Octaacetate

≥98%

Reagent Code: #178153
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CAS Number 4613-78-9

science Other reagents with same CAS 4613-78-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 678.59 g/mol
Formula C₂₈H₃₈O₁₉
badge Registry Numbers
MDL Number MFCD00016917
thermostat Physical Properties
Melting Point 191-195 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. Its fully acetylated structure provides stability and solubility in organic solvents, making it suitable for glycosylation reactions. Commonly employed in the preparation of biologically active glycosides, it serves as a building block in the development of vaccines, antibiotics, and other pharmaceuticals where precise sugar moieties are required. The protecting groups allow for selective deprotection and further functionalization, enabling controlled assembly of sugar chains in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,680.00

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β-D-Gentiobiose Octaacetate
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Used as a key intermediate in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. Its fully acetylated structure provides stability and solubility in organic solvents, making it suitable for glycosylation reactions. Commonly employed in the preparation of biologically active glycosides, it serves as a building block in the development of vaccines, antibiotics, and other pharmaceuticals where precise sugar moieties are required. The protecting groups allo

Used as a key intermediate in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. Its fully acetylated structure provides stability and solubility in organic solvents, making it suitable for glycosylation reactions. Commonly employed in the preparation of biologically active glycosides, it serves as a building block in the development of vaccines, antibiotics, and other pharmaceuticals where precise sugar moieties are required. The protecting groups allow for selective deprotection and further functionalization, enabling controlled assembly of sugar chains in synthetic pathways.

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