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Structure of 193274-82-7
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tert-Butyl 3-benzyl-4-oxopiperidine-1-carboxylate features a sterically shielded tert-butyl ester and a benzyl-substituted piperidinone core, enabling straightforward functionalization at the C4 carbonyl. This scaffold integrates readily into complex heterocycles, offering high stability under standard bench conditions and compatibility with diverse synthetic transformations in medicinal chemistry workflows.
tert-Butyl 3-benzyl-4-oxopiperidine-1-carboxylate serves as a versatile scaffold for the synthesis of piperidine-based heterocycles, enabling efficient access to medicinally relevant cores. The ketone functionality at C4 facilitates nucleophilic addition and reductive amination, while the benzyl group provides orthogonal protection and stability under standard reaction conditions. The tert-butyl carbamate (Boc) group offers convenient deprotection and functionalization, supporting diverse downstream transformations 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: