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Structure of 4897-68-1
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1-Bromo-2-iodo-4-methoxybenzene features a strategically positioned bromo and iodo substituent flanking a methoxy group on a benzene ring, enabling selective cross-coupling reactions. The electron-donating methoxy moiety enhances reactivity in palladium-catalyzed transformations while maintaining stability under standard conditions. This aryl halide serves as a key intermediate for synthesizing functionalized biaryls and heterocyclic scaffolds in medicinal chemistry and materials science.
1-Bromo-2-iodo-4-methoxybenzene serves as a versatile dihalogenated aromatic building block for palladium-catalyzed cross-coupling reactions. The bromo and iodo substituents enable sequential functionalization, while the methoxy group provides orthogonal reactivity and enhances solubility. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for constructing complex aryl 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: