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Structure of 57103-15-8
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9-(4-Iodophenyl)-9H-carbazole is a bench-stable, electron-rich carbazole derivative featuring a para-iodophenyl group at the 9-position. This substitution enhances its utility in cross-coupling reactions, enabling efficient integration into conjugated polymers and organic semiconductors. The iodide moiety serves as a reactive handle for palladium-catalyzed transformations.
9-(4-Iodophenyl)-9H-carbazole serves as a versatile building block for cross-coupling reactions, enabling efficient construction of biaryl systems in medicinal chemistry and materials science. The iodophenyl group exhibits high reactivity in Pd-catalyzed coupling processes such as Suzuki, Stille, and Negishi reactions, while the carbazole core provides structural rigidity and electronic stability. Bench-stable and readily purified by column chromatography, it functions reliably in multi-step syntheses requiring orthogonal functionalization.
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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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: