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Structure of 172913-96-1
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(S)-tert-Butyl (6-oxopiperidin-3-yl)carbamate features a chiral piperidinone core with a bench-stable carbamate protecting group, enabling direct incorporation into complex scaffolds. This configuration supports stereoselective synthesis of bioactive alkaloids and peptide mimetics, where the oxo functionality serves as a key handle for downstream transformations.
(S)-tert-Butyl (6-oxopiperidin-3-yl)carbamate serves as a key chiral building block in the synthesis of piperidine-based scaffolds, enabling efficient access to biologically relevant heterocycles. The protected amine and ketone functionalities provide orthogonal reactivity for sequential transformations. Its bench-stable nature and compatibility with standard coupling, reduction, and cyclization protocols facilitate streamlined synthesis of complex targets in medicinal chemistry and process development 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-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: