Bis(2-diphenylphosphinophenyl) ether; DPEphos

Product Details

CAS No:166330-10-5

MF:C36H28OP2

Appearance:white or off-white crystalline powder

Specification:98.5%

UN number:-

Package:1/5/10/25kgs/drum

Supply Capacity:Tons

Synonyms:1-(diphenylphosphino)-2-(2-(diphenylphosphino)phenoxy)benzene;DPEPHOS [(Oxydi-2,1-phenylene)-bis-(diphenylphosphine)];Bis(2-diphenylphosphinophenyl)ether, 99% DPEphos;Bis(2-diphenylphosphinophenl)ether;{2-[2-(diphenylphosphanyl)phenoxy]phenyl}diphenylphosphane;Bis(2-diphenylphosphinophenyl) ether 98% Min;Bis(2-diphenylphosphinophenyl)ether, 99% 25GR;Bis(2-diphenylphosphinophenyl)ether, 99% 5GR

Product application:Bis(2-diphenylphosphinophenyl) ether, DPEphos, 166330-10-5, Oxydi-2 1-phenylene bis diphenylphosphine, 2 2'-Bis(diphenylphosphino)diphenyl ether, Bidentate phosphine ligand, Organophosphine ligand, Palladium catalyst ligand, Nickel catalyst ligand, Wide bite angle phosphine, Buchwald-Hartwig amination, C-N cross-coupling catalyst, C-C bond formation, C-O coupling reaction, C-S coupling ligand, Pharmaceutical intermediate synthesis, Agrochemical synthesis catalyst, Fine chemical catalysts, Hydroformylation reaction, Carbonylation catalyst, Olefin polymerization, Arylation reactions, High purity DPEphos bulk supplier, Industrial grade DPEphos manufacturer, Organic synthesis reagents

 

Bis(2-diphenylphosphinophenyl) ether serves as an exceptional wide-bite-angle bidentate phosphine ligand widely used in transition metal-catalyzed cross-coupling transformations. In the pharmaceutical industry and active pharmaceutical ingredient (API) development, it coordinates with palladium or nickel complexes to facilitate Buchwald-Hartwig aminations, etherifications, and thioetherifications, significantly streamlining the synthesis of bioactive heterocycles and complex drug intermediates. In agrochemical and fine chemical manufacturing, it delivers outstanding catalytic efficiency and selectivity in diverse carbon-carbon and carbon-heteroatom bond formations, including carbonylation, alkylation, and arylation processes. In the polymer and materials science sectors, it acts as a crucial catalyst component in hydroformylation and olefin polymerization to optimize reaction kinetics and molecular structures. Additionally, bis(2-diphenylphosphinophenyl) ether is instrumental in synthesizing advanced electronic chemicals and organic optoelectronic materials by enabling precise assembly of conjugated conjugated aromatic frameworks.