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Structure of 915226-43-6
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tert-Butyl (R)-3-carbamoylpiperidine-1-carboxylate is a stereochemically defined, bench-stable building block featuring a piperidine core with a carbamoyl group at the 3-position and a tert-butyl ester at the 1-position. This configuration supports efficient incorporation into bioactive molecule synthesis, particularly in medicinal chemistry campaigns requiring chiral piperidine scaffolds. The protected amine and polar carbamoyl moiety enable selective transformations under standard conditions.
tert-Butyl (R)-3-carbamoylpiperidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of piperidine-based pharmaceutical intermediates. Its carbamoyl group enables direct incorporation into bioactive scaffolds, while the tert-butoxycarbonyl (Boc) protection offers excellent bench stability and compatibility with standard peptide coupling and reduction protocols. The compound facilitates efficient access to chiral piperidine derivatives through orthogonal deprotection strategies and demonstrates broad functional group tolerance in multi-step syntheses.
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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: