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Structure of 26670-89-3
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2-Bromo-4-iodo-1-methylbenzene features a strategically positioned methyl group flanked by bromo and iodo substituents, enabling selective cross-coupling reactions. The electron-deficient aromatic ring facilitates palladium-catalyzed transformations, while the halogen pattern supports sequential functionalization. This compound serves as a key intermediate in the synthesis of complex aryl architectures.
2-Bromo-4-iodo-1-methylbenzene serves as a versatile biaryl building block in cross-coupling chemistry, enabling sequential functionalization via Pd-catalyzed reactions. The ortho-bromo and para-iodo substituents provide orthogonal reactivity for iterative coupling strategies, while the methyl group enhances stability and facilitates purification. Its bench-stable nature and compatibility with standard Suzuki, Stille, and Negishi protocols make it ideal for constructing complex aromatic scaffolds in medicinal chemistry and materials science.
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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: