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Structure of 84483-28-3
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2-Chloro-6-iodoaniline features a dual halogenated aromatic core, combining electron-withdrawing chlorine and iodine substituents at ortho positions relative to the amine group. This configuration enables selective cross-coupling reactions in late-stage functionalization, particularly in palladium-catalyzed processes. The molecule exhibits enhanced stability under standard bench conditions and facilitates efficient incorporation into complex heterocyclic scaffolds.
2-Chloro-6-iodoaniline serves as a versatile building block for the synthesis of functionalized aromatic scaffolds, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The chloro and iodo groups facilitate sequential transformations, with the iodo moiety typically reacting first under mild conditions. Its stability under standard bench handling and compatibility with diverse reaction conditions make it a practical choice for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : 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-H319
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Precautionary Statements : P264-P270-P280-P330-P405-P501
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Lot numbers can be found on the outside label of a product: