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Structure of 69411-06-9
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4-Chloro-2,6-difluoroaniline delivers a trifunctional aryl scaffold with orthogonal reactivity. The electron-deficient aromatic ring enables efficient coupling in cross-coupling and amide formation reactions. This bench-stable derivative integrates readily into pharmaceutical intermediates and functional materials, offering enhanced metabolic stability and controlled electronic tuning through strategic fluorination.
4-Chloro-2,6-difluoroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of heterocyclic scaffolds via electrophilic substitution and coupling reactions. Its ortho-fluoro substituents enhance reactivity in palladium-catalyzed cross-couplings, while the chloro group provides a handle for further functionalization. Bench-stable and compatible with standard purification methods, it facilitates streamlined synthesis of complex molecular architectures.
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GHS Pictogram :
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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-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: