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Structure of 29632-73-3
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2-Bromo-4-iodoaniline features dual halogen substituents on the aromatic ring, enabling selective cross-coupling reactions in pharmaceutical and materials synthesis. This bench-stable derivative combines enhanced reactivity with predictable regiochemistry, facilitating efficient access to complex heterocycles and functionalized biaryl systems under standard conditions.
2-Bromo-4-iodoaniline serves as a versatile building block in cross-coupling chemistry, enabling efficient access to substituted biaryls and heterocycles. The ortho-bromo and para-iodo substituents provide complementary reactivity for sequential Pd-catalyzed coupling reactions. Bench-stable and readily purified by recrystallization, it functions reliably in standard Suzuki, Stille, and Negishi transformations, facilitating the construction of complex scaffolds common in medicinal chemistry and materials science.
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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: