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Structure of 582319-15-1
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2,4-Difluoro-6-iodoaniline delivers a trifunctional aryl scaffold featuring orthogonal reactivity at the iodine and amine sites. The electron-deficient ring enhances coupling efficiency in palladium-catalyzed cross-coupling reactions. Bench-stable under standard conditions, this aniline derivative integrates seamlessly into complex molecular architectures for pharmaceutical and agrochemical discovery.
2,4-Difluoro-6-iodoaniline serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds in medicinal chemistry and materials science. The ortho-fluoro substituents enhance reactivity in Suzuki-Miyaura and Buchwald-Hartwig couplings, while the iodine group provides high chemoselectivity and compatibility with standard reaction conditions. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses requiring functional group tolerance and predictable transformation outcomes.
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: