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Structure of 790667-99-1
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tert-Butyl (2S,4S)-4-hydroxy-2-methylpiperidine-1-carboxylate is a chiral piperidine derivative featuring a bench-stable tert-butyl ester protecting group and a stereodefined hydroxyl moiety. This configuration enables direct incorporation into complex molecular scaffolds requiring precise stereocontrol. The molecule bears a reactive hydroxyl site for downstream functionalization while maintaining stability under standard handling conditions.
tert-Butyl (2S,4S)-4-hydroxy-2-methylpiperidine-1-carboxylate serves as a stereochemically defined chiral building block for the synthesis of bioactive molecules. The pendant hydroxyl group enables facile derivatization via esterification or ether formation, while the protected piperidine core exhibits excellent bench stability and compatibility with standard coupling reactions. Its functional group tolerance supports diverse transformations in medicinal chemistry workflows.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: