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Structure of 932372-99-1
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2-Bromo-5-iodophenol features a phenolic scaffold bearing bromo and iodo substituents at ortho and para positions relative to the hydroxyl group, respectively. This electron-deficient aryl system enables selective coupling reactions in transition-metal-catalyzed transformations. The compound exhibits stability under standard bench conditions and serves as a key intermediate in the synthesis of functionalized aromatic architectures for pharmaceutical and materials applications.
2-Bromo-5-iodophenol serves as a versatile diaryl building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its orthogonal halogen reactivity—bromine readily participates in Suzuki, Stille, and Negishi couplings—while iodine offers high reactivity in Buchwald–Hartwig amination and Sonogashira protocols. The phenolic hydroxyl group provides additional functionality for derivatization or protection, enhancing synthetic flexibility. Bench-stable and amenable to standard purification methods, it facilitates reliable synthesis of complex molecular architectures 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: