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Structure of 320-75-2
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2-Bromo-4-fluoro-6-nitrophenol features a trifunctional aromatic core with bromine, fluorine, and nitro groups positioned for orthogonal reactivity. This electron-deficient phenol integrates readily into cross-coupling cascades and serves as a key intermediate in the synthesis of bioactive heterocycles and functional materials.
2-Bromo-4-fluoro-6-nitrophenol serves as a versatile building block in the synthesis of functionalized heterocycles and pharmaceutical intermediates. Its orthogonal reactivity profile—combining electrophilic bromination, nucleophilic fluorination, and nitro group reduction—enables selective transformations under standard conditions. The compound exhibits good bench stability and facilitates efficient coupling reactions, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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Lot numbers can be found on the outside label of a product: