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Structure of 2613-30-1
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4-Chloro-2,5-difluoroaniline features a trifunctional aromatic core with chlorine and two fluorine substituents positioned for orthogonal reactivity. This electron-deficient aniline derivative enables direct coupling in late-stage functionalization, delivering high regioselectivity in pharmaceutical intermediates. The molecule exhibits enhanced metabolic stability and solubility under standard conditions.
4-Chloro-2,5-difluoroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling the construction of fluorinated aromatic scaffolds. Its ortho-fluoro substitution pattern facilitates directed metalation and subsequent functionalization, while the chloro group offers compatibility with palladium-catalyzed coupling reactions. The compound exhibits good bench stability and is readily purified by recrystallization, supporting its use in multi-step syntheses requiring precise regiocontrol.
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Lot numbers can be found on the outside label of a product: