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Structure of 4214-79-3
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5-Chloro-2(1H)-pyridinone is a bench-stable heterocyclic compound featuring a chlorine substituent at the 5-position and a lactam functionality at C2. This electron-deficient pyridinone scaffold serves as a key building block in medicinal chemistry, enabling direct incorporation into bioactive molecules through nucleophilic substitution or transition-metal-catalyzed coupling reactions.
5-Chloro-2(1H)-pyridinone serves as a versatile building block in medicinal chemistry, enabling efficient construction of bioactive heterocycles through nucleophilic substitution and coupling reactions. Its well-established reactivity at the C5 position facilitates functionalization under mild conditions, while the pyridinone core offers favorable solubility and metabolic stability. The compound exhibits excellent bench stability and is compatible with common protecting group strategies, making it ideal for modular 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: