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Structure of 133430-98-5
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2-Bromo-4-iodophenol features a phenolic hydroxyl group flanked by bromo and iodo substituents at the ortho and para positions, respectively. This arrangement imparts strong electron-withdrawing character and enhances reactivity in cross-coupling processes. The molecule exhibits bench-stable handling under inert conditions and serves as a valuable building block for functionalized aryl scaffolds in medicinal chemistry and materials synthesis.
2-Bromo-4-iodophenol serves as a versatile diaryl building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its orthogonal halogen reactivity allows sequential functionalization via Suzuki, Stille, or Negishi couplings. The phenolic hydroxyl group provides additional handle for derivatization or protection, while the compound exhibits good bench stability and ease of purification, making it well-suited for iterative synthesis in medicinal chemistry and materials 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: