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Structure of 864529-90-8
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This piperidine-substituted dioxaphosphepin features a sterically hindered, bench-stable phosphorus center with enhanced reactivity in cross-coupling transformations. The fused dinaphtho architecture imparts rigidity and electronic tuning, enabling efficient incorporation into catalytic systems for C–P bond formation under mild conditions.
1-((11bR)-2,6-dimethyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)piperidine serves as a sterically encumbered, bench-stable phosphine ligand that facilitates palladium-catalyzed cross-coupling reactions. Its rigid dioxaphosphepin core enhances thermal stability and electron density at phosphorus, enabling efficient Suzuki-Miyaura and Negishi couplings with diverse aryl and heteroaryl halides. The piperidine moiety provides solubility and functional group tolerance, supporting scalable synthesis of complex biaryls and pharmaceutical intermediates.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: