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Structure of 214342-63-9
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4-Bromo-1-methylpyridin-2(1H)-one features a bromine substituent at the C4 position and a methyl group at nitrogen, creating a rigid, electron-deficient heterocyclic scaffold. This configuration enables direct functionalization in cross-coupling reactions, particularly under palladium catalysis, while maintaining stability under standard handling conditions. The molecule serves as a key building block for bioactive heterocycles in medicinal chemistry and materials science applications.
4-Bromo-1-methylpyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo group and electron-deficient pyridine core. The 1-methyl substituent enhances solubility and modulates reactivity, while the lactam functionality provides a handle for further functionalization. Its bench stability and compatibility with standard synthetic protocols make it ideal for constructing 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-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: