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Structure of 83159-91-5
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This silyl-protected oxolane derivative features two tert-butyldimethylsilyl ether groups strategically positioned to stabilize reactive hydroxyl functionalities. The (4S,5R) stereochemistry ensures precise spatial control for downstream synthetic applications. Bench-stable and moisture-tolerant, it integrates seamlessly into complex molecule assembly workflows, particularly in carbohydrate and nucleoside analog synthesis.
(4S,5R)-4-[(tert-Butyldimethylsilyl)oxy]-5-{[(tert-butyldimethylsilyl)oxy]methyl}oxolan-2-one serves as a stereochemically defined, silyl-protected diol precursor in complex carbohydrate and natural product synthesis. Its bench-stable structure enables reliable protection of vicinal hydroxyl groups with orthogonal deprotection profiles, facilitating sequential functionalization in multi-step routes. The molecule functions as a key building block for oxolane-based scaffolds, offering predictable reactivity in glycosylation and coupling reactions under standard 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
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Precautionary Statements : P261-P302+P352
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Lot numbers can be found on the outside label of a product: