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Structure of 92138-35-7
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6-Chloro-3-nitropyridin-2(1H)-one features a fused heterocyclic core with complementary electron-deficient and halogenated functionalities. This configuration enables direct incorporation into synthetic scaffolds via cross-coupling or nucleophilic substitution reactions under standard conditions. The compound exhibits bench-stable handling characteristics and facilitates efficient access to bioactive pyridinone derivatives in medicinal chemistry workflows.
6-Chloro-3-nitropyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling efficient access to nitrogen-containing heterocycles via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The ortho-chloro and nitro groups provide complementary reactivity for sequential functionalization, while the pyridinone scaffold offers enhanced solubility and metabolic stability in bioactive molecules. Its bench-stable crystalline form facilitates handling and purification in multi-step syntheses.
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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: