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Structure of 324769-06-4
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This piperidine derivative features a sterically hindered tert-butyl ester and a ketone-functionalized ring, enabling stable incorporation into complex molecular architectures. The electron-deficient carbonyl group facilitates selective transformations in synthetic sequences.
1,1-Dimethylethyl 3,3-dimethyl-4-oxo-1-piperidinecarboxylate serves as a stable, bench-ready piperidinone building block for medicinal chemistry and process development. The tert-butyl ester group enables facile deprotection under mild acidic conditions, while the 4-oxo functionality supports nucleophilic addition and reductive amination reactions. Its sterically shielded 3,3-dimethyl substitution enhances metabolic stability and reduces undesired side reactions, making it ideal for constructing complex heterocyclic scaffolds in API 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: