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Structure of 937013-66-6
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2-(3-Bromophenyl)-1H-imidazole features a brominated phenyl ring fused to an imidazole core, delivering enhanced electron-withdrawing character and enabling efficient coupling in transition-metal-catalyzed reactions. This bench-stable heterocycle integrates readily into pharmaceutical intermediates and functional materials, offering predictable reactivity under standard conditions.
2-(3-Bromophenyl)-1H-imidazole serves as a versatile building block for constructing biaryl-linked heterocycles in medicinal chemistry and materials science. Its bromine substituent enables palladium-catalyzed cross-coupling reactions such as Suzuki, Stille, and Negishi couplings, facilitating the assembly of complex molecular architectures. The imidazole core provides hydrogen-bonding capability and moderate basicity, enhancing solubility and binding interactions in target-directed synthesis. Bench-stable and readily purified by column chromatography, it functions efficiently in standard synthetic workflows.
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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: