(2R,3S,4S,5R,6S)-2-(Acetoxymethyl)-6-(((2R,3R,4S,5R,6R)-4,5-diacetoxy-2-(acetoxymethyl)-6-bromotetrahydro-2H-pyran-3-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate

97%

Reagent Code: #228942
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CAS Number 4753-07-5

science Other reagents with same CAS 4753-07-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 699.45 g/mol
Formula C₂₆H₃₅BrO₁₇
badge Registry Numbers
MDL Number MFCD00153593
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of complex carbohydrates and glycosyl donors, particularly in the preparation of oligosaccharides and glycoconjugates for pharmaceutical research. Its bromine functionality allows for selective coupling reactions, making it valuable in constructing glycosidic bonds with stereochemical control. Commonly employed in the development of antiviral and antibacterial agents, vaccines, and diagnostic probes where precise sugar moieties are required. Also utilized in chemoenzymatic synthesis and solid-phase oligosaccharide assembly due to its reactivity and stability under various protecting group strategies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,530.00
inventory 250mg
10-20 days ฿6,000.00
inventory 1g
10-20 days ฿16,140.00

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(2R,3S,4S,5R,6S)-2-(Acetoxymethyl)-6-(((2R,3R,4S,5R,6R)-4,5-diacetoxy-2-(acetoxymethyl)-6-bromotetrahydro-2H-pyran-3-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
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Used as an intermediate in the synthesis of complex carbohydrates and glycosyl donors, particularly in the preparation of oligosaccharides and glycoconjugates for pharmaceutical research. Its bromine functionality allows for selective coupling reactions, making it valuable in constructing glycosidic bonds with stereochemical control. Commonly employed in the development of antiviral and antibacterial agents, vaccines, and diagnostic probes where precise sugar moieties are required. Also utilized in chemo

Used as an intermediate in the synthesis of complex carbohydrates and glycosyl donors, particularly in the preparation of oligosaccharides and glycoconjugates for pharmaceutical research. Its bromine functionality allows for selective coupling reactions, making it valuable in constructing glycosidic bonds with stereochemical control. Commonly employed in the development of antiviral and antibacterial agents, vaccines, and diagnostic probes where precise sugar moieties are required. Also utilized in chemoenzymatic synthesis and solid-phase oligosaccharide assembly due to its reactivity and stability under various protecting group strategies.

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