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Structure of 938-39-6
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4-Bromoquinolin-2-one features a bromine substituent at the C4 position of a quinolin-2-one scaffold, introducing a reactive handle for cross-coupling transformations. The electron-deficient quinoline core enhances its utility in transition-metal-catalyzed reactions, while the ketone functionality provides a site for nucleophilic addition or derivatization. This compound serves as a versatile intermediate in medicinal chemistry and materials synthesis.
4-Bromoquinolin-2-one serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling direct functionalization at the C4 position via palladium-catalyzed cross-coupling reactions. Its stability under standard reaction conditions, combined with excellent functional group tolerance, facilitates efficient access to diverse quinolinone-based scaffolds relevant to pharmaceutical development. The molecule functions as a key intermediate for constructing bioactive heterocycles and supports scalable synthesis workflows.
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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: