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Structure of 97443-80-6
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This sterically encumbered brominated benzene derivative features three cyclohexyl groups positioned at the 1,3,5-axes, creating a highly hindered, electron-rich aromatic core. The pendant bromine atom enables facile cross-coupling reactions under standard conditions, facilitating the construction of complex polycyclic architectures in synthetic organic chemistry and materials science applications.
2-Bromo-1,3,5-tricyclohexylbenzene serves as a sterically hindered aryl building block for palladium-catalyzed cross-coupling reactions. Its three cyclohexyl groups provide enhanced solubility and stability under reaction conditions while minimizing undesired side reactions. The bromine substituent enables reliable Suzuki, Stille, and Negishi coupling protocols, facilitating the construction of complex biaryl architectures in medicinal chemistry and materials science applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: