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Structure of 697-90-5
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2,4-Dichloro-6-iodoaniline features a trifunctional aryl scaffold with orthogonal halogen handles, enabling sequential cross-coupling in late-stage diversification. The electron-deficient ring enhances reactivity in Pd-catalyzed transformations, while the iodine moiety serves as a high-efficiency coupling partner. This compound delivers precise structural control in complex molecule assembly.
2,4-Dichloro-6-iodoaniline serves as a versatile building block for the synthesis of heterocyclic scaffolds and functionalized aromatic compounds. The iodine substituent enables palladium-catalyzed cross-coupling reactions, while the dichloro groups provide sites for electrophilic substitution or further functionalization. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal 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 : H317-H319
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: