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Structure of 83800-88-8
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2-(4-Bromophenyl)quinazolin-4(3H)-one features a brominated phenyl group appended to the quinazoline core, enhancing electron-withdrawing character and enabling diverse synthetic transformations. This scaffold exhibits robust stability under standard conditions and serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibition pathways.
2-(4-Bromophenyl)quinazolin-4(3H)-one serves as a versatile building block for the synthesis of biologically active quinazoline derivatives. Its bromo substituent enables palladium-catalyzed cross-coupling reactions, facilitating the construction of complex heterocyclic scaffolds. The molecule exhibits good bench stability and functional group tolerance, making it suitable for iterative medicinal chemistry campaigns and API development 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: