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Structure of 778646-95-0
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This chiral piperidine derivative features a tert-butyl-protected amine and methyl-substituted backbone, enabling straightforward functionalization in asymmetric synthesis. The (2R,4R) stereochemistry ensures high diastereoselectivity in downstream transformations, while the dicarboxylate moiety facilitates selective derivatization under mild conditions.
(2R,4R)-1-tert-Butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate serves as a stereochemically defined chiral building block for the synthesis of bioactive piperidine derivatives. The protected amine and dicarboxylate groups enable selective functionalization and orthogonal transformations. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient access to complex heterocyclic scaffolds in medicinal chemistry campaigns.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: