(2R,3R,4R,5S,6S)-2-(Acetoxymethyl)-6-(4-chloro-3-(4-methoxybenzyl)phenyl)tetrahydro-2H-pyran-3,4,5-triyltriacetate

97%

Reagent Code: #232195
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CAS Number 872980-38-6

science Other reagents with same CAS 872980-38-6

blur_circular Chemical Specifications

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Weight 562.99 g/mol
Formula C₂₈H₃₁ClO₁₀
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of complex organic molecules, particularly in pharmaceutical research as an intermediate for developing bioactive compounds. Its functional groups and stereochemistry make it valuable in constructing chiral building blocks for drug discovery. Commonly employed in glycosylation reactions due to its sugar-like structure, enabling the formation of glycosidic bonds in the development of glycoconjugates and enzyme inhibitors. Also utilized in the preparation of protected sugar derivatives for use in combinatorial chemistry and medicinal chemistry pathways.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿246,400.00
(2R,3R,4R,5S,6S)-2-(Acetoxymethyl)-6-(4-chloro-3-(4-methoxybenzyl)phenyl)tetrahydro-2H-pyran-3,4,5-triyltriacetate
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Used in the synthesis of complex organic molecules, particularly in pharmaceutical research as an intermediate for developing bioactive compounds. Its functional groups and stereochemistry make it valuable in constructing chiral building blocks for drug discovery. Commonly employed in glycosylation reactions due to its sugar-like structure, enabling the formation of glycosidic bonds in the development of glycoconjugates and enzyme inhibitors. Also utilized in the preparation of protected sugar derivative

Used in the synthesis of complex organic molecules, particularly in pharmaceutical research as an intermediate for developing bioactive compounds. Its functional groups and stereochemistry make it valuable in constructing chiral building blocks for drug discovery. Commonly employed in glycosylation reactions due to its sugar-like structure, enabling the formation of glycosidic bonds in the development of glycoconjugates and enzyme inhibitors. Also utilized in the preparation of protected sugar derivatives for use in combinatorial chemistry and medicinal chemistry pathways.

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