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Structure of 158406-99-6
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(S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate features a chiral piperidine core with a bromomethyl handle, enabling stereoselective functionalization in medicinal chemistry. This bench-stable reagent integrates readily into synthesis workflows, delivering high-yielding couplings under mild conditions.
(S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate serves as a versatile chiral building block for the synthesis of bioactive molecules, enabling efficient introduction of piperidine scaffolds with defined stereochemistry. The bromomethyl group facilitates nucleophilic substitution reactions, while the tert-butyl carbamate provides a stable, easily removable nitrogen protecting group. This reagent exhibits excellent bench stability and compatibility with standard coupling protocols, supporting scalable synthesis of pharmaceutical intermediates and functionalized heterocycles.
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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: