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Structure of 51417-13-1
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5-Bromo-1,3-dimethyl-2-pyridone features a brominated pyridone core with methyl groups at positions 1 and 3, delivering enhanced stability and tunable reactivity. This electron-deficient heterocycle integrates readily into cross-coupling reactions and serves as a key scaffold in medicinal chemistry. The bromine moiety enables further functionalization via palladium-catalyzed transformations.
5-Bromo-1,3-dimethyl-2-pyridone serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the 2-pyridone core provides a stable, electron-deficient platform for further functionalization. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to complex pyridone-based scaffolds used in pharmaceutical 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
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Precautionary Statements : P264-P270-P301+P310-P330-P501
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Lot numbers can be found on the outside label of a product: