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Structure of 42016-93-3
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2-Chloro-4-iodoaniline features a chlorinated and iodinated aromatic ring system, enabling selective cross-coupling reactions in pharmaceutical synthesis. The electron-deficient aryl moiety integrates efficiently into complex molecular architectures under standard conditions, offering high functional group tolerance and reliable reactivity in Pd-catalyzed transformations.
2-Chloro-4-iodoaniline serves as a valuable building block for constructing substituted anilines and heterocyclic scaffolds in medicinal chemistry. Its dual halogen functionality enables sequential cross-coupling reactions, facilitating efficient access to complex molecular architectures. The compound exhibits good bench stability and is compatible with standard palladium-catalyzed transformations, offering reliable reactivity in diverse synthetic workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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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-H315-H318-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: