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Structure of 346593-03-1
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1-tert-Butoxycarbonyl-2,2-dimethyl-4-piperidone serves as a protected piperidine scaffold for synthesizing bioactive molecules. The tert-butoxycarbonyl group enables stable incorporation into peptide and heterocyclic frameworks, while the 2,2-dimethyl substitution provides steric shielding and enhanced stability under standard conditions. This derivative streamlines access to functionalized piperidines in medicinal chemistry workflows.
1-tert-Butoxycarbonyl-2,2-dimethyl-4-piperidone serves as a stable, bench-ready building block for the synthesis of substituted piperidines. The Boc-protected amine enables straightforward deprotection under mild acidic conditions, while the gem-dimethyl substitution enhances stereochemical stability and reduces epimerization risk. It functions effectively in reductive amination, nucleophilic displacement, and transition-metal-catalyzed coupling reactions, facilitating access to diverse heterocyclic scaffolds used in medicinal chemistry and process development.
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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
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Precautionary Statements : P264-P270-P280-P301+P310-P302+P352-P305+P351+P338-P330-P332+P313-P337+P313-P362+P364-P501
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Lot numbers can be found on the outside label of a product: