(2R,3S,4S,5R,6S)-2-(acetoxymethyl)-4-(benzyloxy)-6-methoxytetrahydro-2H-pyran-3,5-diyl diacetate

95%

Reagent Code: #230943
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CAS Number 81348-19-8

science Other reagents with same CAS 81348-19-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 410.42 g/mol
Formula C₂₀H₂₆O₉
thermostat Physical Properties
Boiling Point 489.3±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.24±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of complex carbohydrates and glycosyl donors in organic chemistry. Its protected hydroxyl groups allow selective deprotection and coupling reactions, making it valuable in the preparation of oligosaccharides, glycoconjugates, and natural product derivatives. Commonly employed in pharmaceutical research for developing glycosidase inhibitors and antibiotic candidates. Also applied in the construction of biologically active molecules where stereochemical control is critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,100.00
inventory 250mg
10-20 days ฿28,500.00
(2R,3S,4S,5R,6S)-2-(acetoxymethyl)-4-(benzyloxy)-6-methoxytetrahydro-2H-pyran-3,5-diyl diacetate
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Used as a key intermediate in the synthesis of complex carbohydrates and glycosyl donors in organic chemistry. Its protected hydroxyl groups allow selective deprotection and coupling reactions, making it valuable in the preparation of oligosaccharides, glycoconjugates, and natural product derivatives. Commonly employed in pharmaceutical research for developing glycosidase inhibitors and antibiotic candidates. Also applied in the construction of biologically active molecules where stereochemical control is c
Used as a key intermediate in the synthesis of complex carbohydrates and glycosyl donors in organic chemistry. Its protected hydroxyl groups allow selective deprotection and coupling reactions, making it valuable in the preparation of oligosaccharides, glycoconjugates, and natural product derivatives. Commonly employed in pharmaceutical research for developing glycosidase inhibitors and antibiotic candidates. Also applied in the construction of biologically active molecules where stereochemical control is critical.
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