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Structure of 1160574-68-4
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4-Bromo-3-chloro-2-fluorobenzonitrile features a trifluorinated aromatic core with orthogonal halogen handles, enabling precise cross-coupling and functionalization in late-stage diversification. This electron-deficient scaffold integrates readily into complex heterocycles and pharmaceutical intermediates under standard conditions.
4-Bromo-3-chloro-2-fluorobenzonitrile serves as a versatile building block for the synthesis of pharmaceutical intermediates and functionalized heterocycles. Its orthogonal halogenation pattern enables selective cross-coupling reactions, including Pd-catalyzed Suzuki and Negishi couplings, with high chemoselectivity. The nitrile group provides a handle for further functionalization via hydrolysis or nucleophilic addition. Bench-stable and readily purified by column chromatography, it is well-suited for scalable medicinal chemistry workflows.
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Lot numbers can be found on the outside label of a product: