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Structure of 54923-31-8
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5-Bromo-6-methylpyridin-2(1H)-one features a brominated pyridinone core with a methyl group at the 6-position, offering a reactive site for cross-coupling and a polar scaffold for synthetic modification. This bench-stable compound integrates readily into medicinal chemistry campaigns requiring halogenated heterocycles.
5-Bromo-6-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 and electronic modulation. Bench-stable and compatible with standard purification methods, it facilitates efficient synthesis of functionalized heterocycles and API intermediates.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: