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Structure of 1010800-01-7
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This trifluoromethanesulfonamide derivative features a sterically encumbered dioxaphosphepin core that enhances stability and facilitates selective phosphorus incorporation in complex molecular architectures. The naphthyl substituents confer rigidity and electron-rich character, enabling efficient coupling reactions under mild conditions.
N-[(11bR)-2,6-Di-2-naphthalenyl-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,1,1-trifluoromethanesulfonamide serves as a highly stable, bench-ready phosphine oxide reagent that enables efficient stereoselective transformations in catalytic asymmetric synthesis. Its rigid, chiral scaffold imparts excellent stereocontrol in transition-metal-catalyzed couplings and functions effectively in cross-coupling protocols requiring high functional group tolerance and predictable reactivity profiles.
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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-H319-H413
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Precautionary Statements : P264-P273-P280-P302+P352-P362-P501
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Lot numbers can be found on the outside label of a product: