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Structure of 180854-44-8
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This chiral piperidine derivative features a bench-stable, moisture-tolerant scaffold with defined stereochemistry at the 2-position. The tert-butyl and ethyl ester groups enable straightforward functionalization, while the 4-oxo moiety provides a reactive handle for downstream transformations in medicinal chemistry applications.
1-tert-Butyl 2-ethyl (2S)-4-oxopiperidine-1,2-dicarboxylate serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective synthesis of piperidine-based scaffolds. The protected amine and ester functionalities offer orthogonal reactivity, facilitating downstream transformations such as reductive amination, nucleophilic substitution, and ring functionalization. Bench-stable and readily purified by chromatography, it functions effectively in multi-step sequences for medicinal chemistry and natural product 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: