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Structure of 1217753-75-7
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tert-Butyl (S)-3-aminopiperidine-1-carboxylate hydrochloride is a bench-stable, moisture-tolerant chiral building block featuring a protected primary amine and a stereogenic center. This piperidine derivative integrates readily into medicinal chemistry campaigns requiring enantiopure scaffolds. The tert-butyl carbamate group enables selective deprotection under mild acidic conditions, facilitating downstream functionalization in complex molecule synthesis.
tert-Butyl (S)-3-aminopiperidine-1-carboxylate hydrochloride serves as a key chiral building block for the synthesis of bioactive piperidine derivatives. Its protected amine and tertiary amine functionality enable straightforward functionalization in medicinal chemistry workflows, including reductive amination, coupling reactions, and transition-metal-catalyzed transformations. The tert-butyl carbamate group offers excellent bench stability and facilitates easy removal under mild acidic conditions, enabling efficient access to the parent amine scaffold.
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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: