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Structure of 1374030-19-9
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(11bS)-4-Hydroxy-2,6-bis(4-methoxyphenyl)-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin features a chiral phosphorus center with a hydroxyl group and two electron-rich methoxy-substituted aryl moieties. This sterically defined, bench-stable scaffold enables precise stereocontrol in asymmetric synthesis, particularly in catalytic transformations requiring rigid, polarized transition states.
(11bS)-4-Hydroxy-2,6-bis(4-methoxyphenyl)-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin serves as a sterically hindered, bench-stable phosphine oxide scaffold with defined stereochemistry at the 11b position. It functions as a modular building block in asymmetric synthesis, enabling controlled P–C bond formation and facilitating transition-metal-catalyzed cross-coupling reactions. Its orthogonally protected hydroxyl group and electron-rich aryl substituents support diverse functionalization while maintaining structural integrity under standard reaction conditions.
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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+P364
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Lot numbers can be found on the outside label of a product: