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Structure of 97614-43-2
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2-Deoxy-2-fluoro-α-D-arabinofuranose 1,3,5-tribenzoate features a fluorinated sugar core with three benzoate esters enabling enhanced stability and solubility in organic media. This protected nucleoside precursor facilitates efficient glycosylation reactions under mild conditions, serving as a key intermediate in the synthesis of fluorinated glycoconjugates and antiviral agents.
2-Deoxy-2-fluoro-α-D-arabinofuranose 1,3,5-tribenzoate serves as a stable, bench-ready glycosyl donor for stereoselective glycosylation reactions. The 2-fluoro group enhances anomeric control through neighboring group participation, while the tribenzoate protection pattern provides excellent stability and orthogonal deprotection compatibility. It facilitates efficient construction of fluorinated nucleoside analogs and complex oligosaccharides under standard glycosylation conditions.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: