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Structure of 5239-39-4
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6,6-dimethylpiperidine-2,4-dione features a sterically hindered diketone core that enhances stability and modulates reactivity. This bench-stable scaffold integrates readily into synthetic sequences requiring electron-deficient heterocyclic motifs. Its dual carbonyl functionality supports diverse transformations in medicinal chemistry and materials development.
6,6-Dimethylpiperidine-2,4-dione serves as a versatile building block in medicinal chemistry, enabling efficient access to saturated heterocyclic scaffolds via standard enolate chemistry and nucleophilic addition reactions. Its diketone functionality supports controlled functionalization at C2 and C4, while the gem-dimethyl substitution enhances metabolic stability and modulates lipophilicity. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns in API development.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: