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Structure of 117565-57-8
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tert-Butyl 3-ethyl-4-oxopiperidine-1-carboxylate features a sterically hindered piperidinone core with a bench-stable carbamate protecting group. This compound integrates readily into synthetic sequences requiring selective nitrogen functionalization, offering enhanced solubility and stability under standard conditions.
tert-Butyl 3-ethyl-4-oxopiperidine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds. The ketone functionality at C4 supports selective reduction, enolate formation, and nucleophilic addition, while the tert-butoxycarbonyl (Boc) group provides stable protection for nitrogen during multistep synthesis. Its bench-stable nature and compatibility with standard coupling and functionalization protocols facilitate straightforward purification and integration into complex molecular architectures.
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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: