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Structure of 99465-09-5
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5-Bromoquinolin-2(1H)-one features a bromine-substituted quinolinone scaffold with enhanced electrophilicity at the C5 position, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The carbonyl group at C2 provides a stable platform for derivatization, while the electron-deficient aromatic system supports efficient metal-catalyzed transformations under mild conditions. This compound serves as a key building block in medicinal chemistry and materials synthesis.
5-Bromoquinolin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine handle. The quinolinone core provides inherent stability and facilitates incorporation into bioactive scaffolds. Its functional group tolerance supports sequential transformations, while the carbonyl moiety enhances solubility and crystallinity, simplifying purification and isolation.
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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: