(2R,3S,4S,5R,6S)-2-(Acetoxymethyl)-6-(4-(hydroxymethyl)-2-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
97%
Reagent
Code: #228964
CAS Number
290298-12-3
blur_circular Chemical Specifications
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Molecular Information
Weight
499.42 g/mol
Formula
C₂₁H₂₅NO₁₃
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Registry Numbers
MDL Number
MFCD31731121
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Storage & Handling
Storage
-20°C, Inert Gas
description Product Description
Used primarily as an intermediate in the synthesis of glycosylation agents for pharmaceutical applications, particularly in the preparation of complex carbohydrate structures. Its protected hydroxyl and reactive acetoxy groups allow selective reactions in the construction of oligosaccharides used in vaccine development and antibiotic synthesis. The nitro group facilitates further functionalization through reduction to an amino group, enabling conjugation with other biomolecules. Commonly employed in research settings for developing glycoconjugate vaccines and studying enzyme substrates.
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(2R,3S,4S,5R,6S)-2-(Acetoxymethyl)-6-(4-(hydroxymethyl)-2-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
Used primarily as an intermediate in the synthesis of glycosylation agents for pharmaceutical applications, particularly in the preparation of complex carbohydrate structures. Its protected hydroxyl and reactive acetoxy groups allow selective reactions in the construction of oligosaccharides used in vaccine development and antibiotic synthesis. The nitro group facilitates further functionalization through reduction to an amino group, enabling conjugation with other biomolecules. Commonly employed in research settings for developing glycoconjugate vaccines and studying enzyme substrates.
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