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Structure of 1245646-10-9
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tert-Butyl 4-hydroxy-2-oxopiperidine-1-carboxylate features a sterically hindered tert-butyl ester and a reactive ketone moiety, enabling direct functionalization at the C4 position. The hydroxyl group enhances solubility and facilitates downstream derivatization. This bench-stable scaffold integrates readily into complex heterocyclic architectures.
tert-Butyl 4-hydroxy-2-oxopiperidine-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to piperidine-based scaffolds. The hydroxyl group facilitates selective derivatization, while the oxo function supports nucleophilic addition and reductive transformations. Its tert-butyl carbamate handle provides stability and ease of removal under mild acidic conditions, making it ideal for iterative synthesis 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: