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Structure of 116130-33-7
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2-Chloro-4-iodophenol features a phenolic hydroxyl group flanked by chlorine and iodine substituents, enabling selective coupling reactions in medicinal chemistry. The electron-withdrawing halogens enhance reactivity in palladium-catalyzed cross-couplings while maintaining stability under standard conditions. This scaffold serves as a key building block for bioactive molecule synthesis.
2-Chloro-4-iodophenol serves as a valuable building block in the synthesis of functionalized aromatic scaffolds, enabling direct coupling reactions via its orthogonal halogenation pattern. The chloro group facilitates palladium-catalyzed cross-coupling, while the iodo substituent offers high reactivity in Suzuki, Stille, and Negishi transformations. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for iterative medicinal chemistry campaigns and API intermediate development.
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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: