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Structure of 156772-63-3
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5-Bromo-3-fluoropyridin-2(1H)-one features a fused heterocyclic core with complementary halogen substituents enabling precise functionalization. The bromine at C5 and fluorine at C3 facilitate cross-coupling reactions, while the lactam carbonyl enhances solubility and stability under standard conditions. This scaffold integrates readily into bioactive molecules for medicinal chemistry applications.
5-Bromo-3-fluoropyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine functionality. The fluorine substituent enhances metabolic stability and modulates electronic properties. Its pyridinone core provides hydrogen-bonding capability and facilitates incorporation into bioactive heterocycles. Bench-stable and compatible with standard purification methods, it functions effectively in the synthesis of kinase inhibitors and other pharmaceutical scaffolds.
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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: