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Structure of 128259-68-7
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1,3-Dibromo-2,5-difluorobenzene features a highly functionalized aromatic core with bromine and fluorine substituents positioned for orthogonal reactivity. This electron-deficient scaffold enables selective cross-coupling transformations under palladium catalysis, offering access to complex fluorinated biaryls. The molecule exhibits enhanced stability and compatibility with standard reaction conditions.
1,3-Dibromo-2,5-difluorobenzene serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The difluoro substitution enhances metabolic stability and modulates electronic properties, while the dibromo functionality offers sequential functionalization potential. Bench-stable and compatible with standard reaction conditions, it facilitates efficient construction of fluorinated aromatic scaffolds relevant to medicinal chemistry and materials science.
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Lot numbers can be found on the outside label of a product: