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Structure of 91547-59-0
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1,2-Dideoxy-D-ribofuranose is a key carbohydrate scaffold lacking hydroxyl groups at the 1 and 2 positions, conferring enhanced stability and reduced reactivity. This configuration enables selective functionalization at C3 and C4, facilitating use in glycosylation studies and nucleoside analog synthesis. The furanose ring maintains conformational rigidity under standard conditions, supporting precise stereochemical control in synthetic pathways.
1,2-Dideoxy-D-ribofuranose serves as a key building block in carbohydrate chemistry, enabling the synthesis of nucleoside analogs and glycosylation intermediates. Its stable furanose ring and defined stereochemistry facilitate selective functionalization at C3 and C4 positions. The absence of hydroxyl groups at C1 and C2 enhances its stability under acidic conditions and simplifies purification, making it valuable for constructing complex oligosaccharides and evaluating glycosidase substrate specificity in medicinal and biochemical research.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: