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Structure of 884494-94-4
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3-Bromo-5-fluoropyridin-2(1H)-one features a fused heterocyclic core bearing strategically positioned halogen substituents, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The electron-deficient pyridinone scaffold enhances reactivity toward amines and thiols, while the bromine and fluorine atoms provide orthogonal handles for sequential derivatization. This bench-stable compound integrates readily into complex molecular architectures used in medicinal chemistry and materials science.
3-Bromo-5-fluoropyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal reactivity profile. The bromo group facilitates C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the fluorine and lactam functionalities provide enhanced metabolic stability and hydrogen-bonding capacity. Its bench-stable crystalline nature simplifies handling and purification, making it ideal for modular synthesis of bioactive heterocycles and API intermediates.
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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: