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Structure of 21740-00-1
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5-Bromo-2-iodobenzoic acid features a benzoic acid core functionalized with bromo and iodo substituents at the meta and ortho positions, respectively. This dual halogenation enables efficient cross-coupling transformations in synthetic routes. The carboxylic acid group facilitates derivatization and incorporation into bioactive scaffolds. Designed for use in medicinal chemistry and materials synthesis, this compound offers high reactivity under standard palladium-catalyzed conditions.
5-Bromo-2-iodobenzoic acid serves as a versatile dihalogenated aromatic building block for palladium-catalyzed cross-coupling reactions. The bromo and iodo groups enable sequential functionalization via orthogonal reactivity, facilitating the assembly of complex biaryl architectures. Its carboxylic acid functionality offers direct handle for derivatization, while maintaining bench stability and compatibility with standard purification protocols in medicinal chemistry and materials synthesis workflows.
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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: