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Structure of 344-19-4
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2,6-Dichloro-4-fluoroaniline features a trifunctional aromatic core with chlorine and fluorine substituents positioned for orthogonal reactivity. This electron-deficient aniline derivative enables selective coupling in pharmaceutical intermediates and agrochemical scaffolds. The para-fluoro group enhances metabolic stability, while the ortho-chlorines direct electrophilic substitution patterns. Bench-stable under standard conditions, it integrates readily into complex molecular architectures.
2,6-Dichloro-4-fluoroaniline serves as a valuable building block in medicinal chemistry and agrochemical synthesis, enabling the construction of diverse heterocyclic scaffolds. Its orthogonal halogenation pattern facilitates selective cross-coupling reactions, while the amine group provides a handle for direct derivatization. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for multi-step synthetic sequences in industrial R&D workflows.
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GHS No : GHS06,GHS08,GHS09
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301+H311+H331-H373-H411
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Precautionary Statements : P261-P273-P280
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Lot numbers can be found on the outside label of a product: