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Structure of 22362-86-3
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9-Iodoanthracene serves as a key electrophilic coupling partner in palladium-catalyzed cross-coupling reactions. The iodine substituent enables efficient C–C bond formation under mild conditions, while the planar anthracene core provides enhanced π-conjugation for applications in organic semiconductors and optoelectronic materials. This compound exhibits excellent stability and solubility in common organic solvents.
9-Iodoanthracene serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and extended π-conjugated systems. Its iodine functionality exhibits high reactivity under standard Pd(0)-catalyzed conditions, facilitating reliable C–C bond formation with arylboranes, stannanes, and other coupling partners. The anthracene core provides inherent rigidity and planarity, enhancing electronic communication in optoelectronic applications. Bench-stable and readily purified by recrystallization, it functions effectively in both academic and industrial synthetic workflows.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H400-H410
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Precautionary Statements : P264-P270-P273-P391-P501
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Lot numbers can be found on the outside label of a product: