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Structure of 1133123-02-0
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4-Bromo-2-iodobenzoic acid features a benzoic acid core with strategically positioned bromo and iodo substituents, enabling efficient transition metal-catalyzed cross-coupling reactions. The electron-deficient aromatic ring facilitates palladium-mediated transformations, while the carboxylic acid group provides a handle for derivatization or conjugation in synthetic sequences. This compound serves as a key intermediate in the synthesis of functionalized biaryl systems and pharmaceutical scaffolds.
4-Bromo-2-iodobenzoic acid serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its orthogonal halogen reactivity—bromine typically undergoing Suzuki or Stille coupling while iodine participates in faster Negishi or Sonogashira transformations—facilitates sequential functionalization. The carboxylic acid group supports direct derivatization or acts as a handle for further synthetic elaboration, offering enhanced solubility and purification advantages in multi-step synthesis.
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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
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Precautionary Statements : P264-P270-P301+P310-P330-P501
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Lot numbers can be found on the outside label of a product: