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Structure of 861601-15-2
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1-Bromo-3-iodo-5-nitrobenzene features ortho-halogenated positions flanking a strong electron-withdrawing nitro group, enabling selective cross-coupling in late-stage functionalization. The bromine and iodine sites offer complementary reactivity in palladium-catalyzed transformations, facilitating sequential derivatization under mild conditions. This aryl halide exhibits excellent stability during storage and handling, making it ideal for complex molecule assembly in medicinal chemistry and materials synthesis.
1-Bromo-3-iodo-5-nitrobenzene serves as a versatile dihalogenated aromatic building block for palladium-catalyzed cross-coupling reactions. The bromo and iodo substituents enable sequential functionalization, while the nitro group provides strong electron-withdrawal and ortho-directing effects. Its bench-stable nature and compatibility with standard Suzuki, Stille, and Negishi coupling conditions make it ideal for constructing complex aryl scaffolds 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: