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Structure of 1804897-66-2
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3-Bromo-4-chloropyridin-2(1H)-one features a fused heterocyclic core with complementary halogen handles, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The electron-deficient pyridinone scaffold enhances reactivity toward amines and thiols, while maintaining bench-stable handling under standard conditions.
3-Bromo-4-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 Suzuki, Stille, and Negishi couplings, while the chloro substituent offers enhanced stability and selective functionalization. Its pyridinone core provides hydrogen-bonding capacity and structural rigidity, making it suitable for constructing bioactive heterocycles and API intermediates with predictable solubility and handling characteristics.
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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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: