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Structure of 791616-59-6
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This sterically encumbered phosphine oxide features a rigid dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin core with a (11bR)-configured hydroxy group and two para-trifluoromethylphenyl substituents. The electron-withdrawing trifluoromethyl groups enhance oxidative stability while the oxygenated scaffold promotes solubility in polar organic media. This structure enables efficient coupling reactions under mild conditions.
(11bR)-4-Hydroxy-2,6-bis[4-(trifluoromethyl)phenyl]-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin serves as a sterically encumbered, bench-stable phosphine oxide scaffold with enhanced oxidative stability. Its structure enables controlled reactivity in transition-metal-catalyzed cross-coupling processes, particularly in Pd-catalyzed Suzuki-Miyaura and Negishi reactions. The trifluoromethyl aryl groups confer high electron-withdrawing character and improve solubility in organic media, facilitating purification and handling during multi-step synthesis of complex heterocyclic systems and functionalized scaffolds.
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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-P280-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: