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Structure of 116369-24-5
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4-Bromo-5-chloro-2-fluoroaniline features a trihalogenated aromatic core with strategic electronic modulation. The ortho-fluoro and meta-bromo substituents enhance reactivity in cross-coupling processes, while the para-chloro group provides a stable handle for downstream functionalization. This bench-stable intermediate enables efficient access to complex heterocyclic architectures in medicinal chemistry and materials science.
4-Bromo-5-chloro-2-fluoroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling the construction of complex heterocyclic scaffolds via standard coupling reactions. Its ortho-halogenated arylamine core facilitates palladium-catalyzed cross-couplings and direct arylation processes. The molecule exhibits good bench stability, moderate solubility in common organic solvents, and tolerates a range of functional groups, making it well-suited for multi-step synthetic sequences requiring precise regiocontrol and reactivity.
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Lot numbers can be found on the outside label of a product: