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Structure of 695162-87-9
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This sterically encumbered dioxaphosphepin features a chiral 11bR configuration and a hydroxylated, electron-deficient phosphorus center. The ortho-methylated aryl substituents confer exceptional stability and solubility in nonpolar media, enabling robust performance in asymmetric catalysis and transition-metal-free phosphorylation reactions under ambient conditions.
(11bR)-4-Hydroxy-2,6-bis(2,4,6-trimethylphenyl)-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin serves as a sterically encumbered, bench-stable phosphine oxide with enhanced oxidative stability. It functions as a robust ligand in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ortho-substituted aryl groups confer high functional group tolerance and facilitate easy purification, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
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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
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: