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Structure of 1630197-34-0
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4-Bromo-5-methoxypyridin-2(1H)-one features a bromine substituent at the 4-position and a methoxy group at the 5-position on a pyridinone scaffold. This electron-deficient heterocycle integrates readily into cross-coupling reactions, offering high functional group tolerance and stability under standard conditions.
4-Bromo-5-methoxypyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo substituent. The pyridinone core provides hydrogen-bonding capacity and enhanced solubility, while the methoxy group offers moderate electronic modulation. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative synthesis of heterocyclic scaffolds and API intermediates.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: