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Structure of 1805590-93-5
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5-Bromo-4-fluoropyridin-2(1H)-one features a uniquely reactive pyridinone core bearing bromo and fluoro substituents at the 5- and 4-positions, respectively. This combination enables selective cross-coupling transformations while maintaining stability under standard reaction conditions. The molecule's electron-deficient heterocyclic framework facilitates efficient functionalization in medicinal chemistry and materials synthesis workflows.
5-Bromo-4-fluoropyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C5 position via cross-coupling reactions. The fluorine substituent enhances metabolic stability and modulates electronic properties, while the pyridinone core provides hydrogen-bonding capacity and facilitates metal coordination. Its bench-stable nature and compatibility with palladium-catalyzed transformations make it ideal for constructing complex heterocyclic scaffolds in API development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: