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Structure of 570391-20-7
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3-Bromo-5-iodophenol features a phenolic hydroxyl group flanked by bromo and iodo substituents at the meta and para positions, respectively. This electronic asymmetry enables selective coupling in cross-coupling reactions. The molecule exhibits enhanced stability under standard conditions and serves as a valuable building block for functionalized aryl scaffolds in medicinal chemistry and materials synthesis.
3-Bromo-5-iodophenol serves as a versatile diaryl building block for Suzuki-Miyaura and Stille coupling reactions, enabling the construction of biaryl scaffolds under mild conditions. The bromo and iodo substituents exhibit complementary reactivity profiles, allowing sequential functionalization with high regiocontrol. Its phenolic functionality offers direct access to hydroxylated heterocycles and facilitates downstream derivatization via etherification or metal-catalyzed cross-coupling. The compound demonstrates excellent bench stability and is readily purified by recrystallization or flash chromatography, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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: