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Structure of 1170736-59-0
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This sterically encumbered dioxaphosphepin features a hydroxylated oxide bridge and two 3,5-dimethylphenyl substituents at the 2,6-positions, delivering enhanced stability and solubility in polar organic media. The chiral (11bS) configuration ensures high stereoselectivity in asymmetric catalysis applications.
(11bS)-2,6-Bis(3,5-dimethylphenyl)-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin serves as a sterically hindered, bench-stable phosphine oxide scaffold that facilitates stereoselective transformations in catalytic systems. Its rigid, electron-rich architecture enables efficient ligand coordination in transition-metal catalysis and supports functional group tolerance in multistep syntheses. The molecule’s defined stereochemistry and oxidative stability make it a reliable building block for asymmetric synthesis and catalyst development.
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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: