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Structure of 169457-73-2
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Tert-butyl 4-(2-bromoethyl)piperidine-1-carboxylate features a piperidine core bearing a tert-butyl carbamate protecting group and a pendant bromoethyl chain. This bifunctional scaffold enables direct alkylation or transition-metal-catalyzed coupling reactions, serving as a key intermediate in the synthesis of bioactive molecules and pharmaceutical candidates. The robust protecting group ensures stability under diverse reaction conditions.
Tert-butyl 4-(2-bromoethyl)piperidine-1-carboxylate serves as a versatile building block for constructing piperidine-based scaffolds in medicinal chemistry. The bromoethyl side chain enables efficient nucleophilic substitution, facilitating the installation of diverse functional groups or heterocyclic extensions. The tert-butyl carbamate protects the piperidine nitrogen under standard reaction conditions, offering excellent bench stability and compatibility with common coupling protocols. Its reactivity profile supports straightforward derivatization for API intermediates and target molecule synthesis.
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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: