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Structure of 872998-61-3
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2,4-Dibromoquinazoline serves as a key building block in medicinal chemistry, featuring two bromine substituents at electron-rich positions that enable efficient palladium-catalyzed cross-coupling reactions. This stable, bench-ready heterocycle integrates readily into complex scaffolds for kinase inhibitor development and functional materials synthesis.
2,4-Dibromoquinazoline serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of biaryl and heterocyclic scaffolds. The dibromo substitution pattern provides high reactivity in Suzuki, Stille, and Negishi couplings, facilitating rapid diversification of quinazoline cores. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for iterative synthesis campaigns targeting kinase inhibitors and other bioactive molecules.
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Lot numbers can be found on the outside label of a product: