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Structure of 880094-83-7
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5-Bromo-3,4-dihydro-2(1H)-quinolinone features a brominated quinolinone core with enhanced electrophilicity at the C5 position. This scaffold integrates readily into transition-metal-catalyzed couplings and serves as a key intermediate in medicinal chemistry. The compound exhibits excellent stability under standard conditions and facilitates efficient derivatization for drug discovery applications.
5-Bromo-3,4-dihydro-2(1H)-quinolinone serves as a versatile building block in medicinal chemistry, enabling late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the saturated quinolinone core offers favorable solubility and stability under standard reaction conditions. Its well-defined regiochemistry facilitates predictable transformations, making it ideal for constructing complex heterocyclic scaffolds in API development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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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: