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Structure of 1135531-73-5
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2-Bromo-4-chloro-6-fluorobenzaldehyde features a trifluorinated aromatic core with strategically positioned halogens enabling direct functionalization in cross-coupling reactions. The aldehyde group provides a handle for nucleophilic addition and condensation chemistry, while the electron-withdrawing halogens enhance reactivity. This compound serves as a key intermediate in pharmaceutical synthesis, offering high stability under standard bench conditions.
2-Bromo-4-chloro-6-fluorobenzaldehyde serves as a versatile building block in the synthesis of substituted heterocycles and bioactive molecules. Its orthogonal halogenation pattern enables sequential cross-coupling reactions, while the aldehyde functionality facilitates imine formation, reductive amination, or condensation cascades. Bench-stable and readily purified by recrystallization, it functions reliably in Pd-catalyzed coupling protocols and is well-suited for iterative synthetic strategies in medicinal chemistry and agrochemical development.
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Lot numbers can be found on the outside label of a product: