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Structure of 848423-85-8
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3-Bromo-6-chloropyridin-2(1H)-one features a dual halogenated pyridinone core with orthogonal reactivity, enabling selective functionalization in late-stage diversification. The electron-deficient ring facilitates nucleophilic substitution, while the carbonyl group provides anchoring for transition metal catalysis. This scaffold integrates readily into bioactive molecule architectures under standard conditions.
3-Bromo-6-chloropyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromo group facilitates efficient Suzuki, Stille, or Negishi couplings, while the chloro substituent remains inert under standard conditions. Its stability under ambient storage and compatibility with diverse functional groups make it ideal for constructing complex heterocyclic scaffolds in API development.
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Lot numbers can be found on the outside label of a product: