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Structure of 217309-46-1
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This tetrahydrofuro[3,4-d][1,3]dioxole features a silyl-protected hydroxyl group and a geminal dimethyl motif, enabling stable incorporation into complex carbohydrate syntheses. The tert-butyldimethylsilyl moiety provides robust protection under standard conditions, while the rigid fused ring system supports stereoselective transformations.
(3aR,6R,6aR)-6-(((tert-Butyldimethylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol serves as a stereochemically defined, bench-stable building block for complex carbohydrate and nucleoside synthesis. The silyl ether group provides robust protection of the C6 hydroxyl, enabling orthogonal deprotection in multi-step sequences. Its rigid tetrahydrofuro[3,4-d][1,3]dioxole core supports reliable glycosylation reactions and functions as a key intermediate in the construction of bioactive heterocyclic scaffolds requiring precise stereocontrol.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: