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Structure of 1227578-85-9
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4-Bromo-5-methylpyridin-2(1H)-one features a pyridinone core with bromo and methyl substituents at the 4- and 5-positions, respectively. This electron-deficient heterocycle enables direct functionalization in cross-coupling reactions. The compound exhibits bench-stable handling and compatibility with palladium-catalyzed transformations, facilitating rapid access to substituted pyridine scaffolds for medicinal chemistry applications.
4-Bromo-5-methylpyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The pyridinone core provides hydrogen-bonding capability and enhanced solubility, while the methyl group offers mild steric influence. This compound exhibits good bench stability and facilitates efficient functionalization in standard synthetic workflows, making it suitable for constructing heterocyclic scaffolds relevant to 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-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: