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Structure of 6052-73-9
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5,6-Dihydropyridin-2(1H)-one features a reduced pyridinone core with enhanced nucleophilicity at the C5 position, enabling direct functionalization in synthetic transformations. This scaffold integrates readily into heterocyclic architectures and serves as a key intermediate in medicinal chemistry applications.
5,6-Dihydropyridin-2(1H)-one serves as a versatile scaffold in medicinal chemistry, enabling efficient access to functionalized pyridine derivatives. Its enolizable carbonyl and conjugated diene system facilitate Diels-Alder reactions, nucleophilic additions, and transition-metal-catalyzed couplings. The compound exhibits bench stability and compatible functional group tolerance, supporting straightforward purification and integration into multi-step syntheses of heterocyclic drug candidates.
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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: