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Structure of 945907-32-4
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1-(3-Bromo-4-iodophenyl)ethan-1-one features a dual halogenated aryl core with bromine and iodine positioned ortho to each other on the phenyl ring, enabling selective cross-coupling reactions. The ketone functionality provides a handle for further derivatization, while the molecule exhibits stability under standard bench conditions and compatibility with palladium-catalyzed transformations.
1-(3-Bromo-4-iodophenyl)ethan-1-one serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds. The ortho-bromo and para-iodo substituents provide orthogonal reactivity for sequential functionalization. Its bench-stable ketone functionality offers compatibility with diverse reaction conditions, facilitating downstream derivatization in medicinal chemistry and materials synthesis.
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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: