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Structure of 1821720-33-5
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This chiral tetrahydropyran alcohol features a rigid, oxygen-containing ring with defined stereochemistry at the 2- and 4-positions. The methyl group at C2 imparts steric bias, while the hydroxyl at C4 enables selective derivatization. Bench-stable and moisture-tolerant, this scaffold integrates readily into complex molecular architectures for natural product synthesis and medicinal chemistry applications.
(2R,4R)-2-methyltetrahydro-2H-pyran-4-ol serves as a chiral building block for the synthesis of bioactive molecules, offering predictable stereocontrol in glycosylation and cyclization reactions. Its bench-stable, crystalline nature facilitates handling and purification, while the hydroxyl and methyl groups enable selective functionalization. Functions as a key intermediate in carbohydrate mimetics and natural product derivatives.
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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: