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Structure of 1043567-32-3
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This sterically encumbered phosphine oxide features a rigid, polycyclic framework that enhances thermal stability and resistance to oxidation. The 4-hydroxy group enables hydrogen bonding and modulates electronic properties, while the phenanthrenyl substituents provide extended π-conjugation and steric shielding around the phosphorus center. This structure facilitates controlled coordination in catalytic systems and improves performance in air-sensitive transformations under standard bench conditions.
(11bS)-4-Hydroxy-2,6-di(phenanthren-9-yl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide serves as a sterically encumbered, bench-stable phosphine oxide scaffold with defined stereochemistry at the 11b position. It functions as a versatile building block in transition-metal-catalyzed cross-coupling reactions and enables precise control in the synthesis of complex polycyclic architectures. Its hydroxyl group provides a handle for derivatization, while the phenanthrene substituents enhance rigidity and electronic modulation, offering improved functional group tolerance and reproducibility in catalytic systems.
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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: