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Structure of 1226860-66-7
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3-Bromo-9-(4-bromophenyl)-9H-carbazole features a carbazole core functionalized with bromine atoms at the 3-position and para to a phenyl ring, enabling efficient coupling in cross-coupling reactions. The electron-rich aromatic system enhances reactivity in palladium-catalyzed transformations. This structure supports modular synthesis of conjugated materials for optoelectronic applications.
3-Bromo-9-(4-bromophenyl)-9H-carbazole serves as a versatile building block for constructing carbazole-based scaffolds in medicinal chemistry and materials science. The molecule features two bromine substituents at regioselective positions, enabling efficient palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Stille couplings. Its bench-stable, crystalline nature facilitates handling and purification, while the electron-rich carbazole core supports diverse functionalization. This compound functions effectively in the synthesis of advanced organic semiconductors and potential kinase inhibitors.
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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: