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    136705-75-4

    Catalog No. EBD3043913

    CAS 136705-75-4

    Name (-)-1,2(2R,5R)-2,5-(DIMETHYLPHOSPHOLANO)BENZENE(CYCLOOCTADIENE)RHODIUM(I)TRIFLUOROMETHANESULFONATE

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    Basic Information

    Synonyms: (S,S)-ME-DUPHOS-R (S,S)-ME-DUPHOS-RH 1,2-BIS((2S,5S)-2,5-DIMETHYLPHOSPHOLANO& BISDIMETHYLPHOSPHOLANOBENZENECYCLOOCTADIENERHODIUMTRIFLUOROMETHANESULF (+)-1,2-BIS((2S,5S)-DIMETHYLPHOSPHOLANO)BENZENE(CYCLOOCTADIENE)RHODIUM(I)TRIFLATE (+)-1,2-BIS[(2S,5S)-DIMETHYLPHOSPHOLANO)BENZENE(CYCLOOCTADIENE]RHODIUM(I)TRIFLATE,96% (-)-1,2-BIS((2R,5R)-2,5-DIMETHYLPHOSPHOLANO)BENZENE(CYCLOOCTADIENE)RHODIUM(I)TRIFLUOROMETHANESULFON (+)-1,2-Bis((2S,5S)-2,5-dimethylphospholano)benzene(cyclooctadiene)rhodium(I)trifluoromethanesulfonate

    Molecular Formula: C27H40F3O3P2RhS

    Molecular Weight: 666.52

    Categories: Synthetic Chemistry > Catalysts and Ligands > Metal-Ligand Complexes Materials Chemistry > Optoelectronic and Organic Semiconductor Materials > Optoelectronic Functional Compounds

    Product Description:
    This compound, with CAS number 136705-75-4, is a rhodium(III) complex coordinated by two (2S,5S)-2,5-dimethylphospholane ligands and a trifluoromethanesulfonate (triflate) anion. It is formally known as (+)-1,2-Bis((2S,5S)-2,5-dimethylphospholanyl)benzene(trifluoromethanesulfonato)rhodium. The structure features a chiral, electron-rich bis(phospholane) ligand framework, which is key to its function. Its primary and most significant application is as a highly efficient and enantioselective homogeneous catalyst for hydrogenation reactions. Specifically, it is renowned for the asymmetric hydrogenation of dehydroamino acid derivatives and enamides to produce chiral α-amino acids and their derivatives with very high enantiomeric excess (ee). This makes it a critical tool in the synthesis of pharmaceutical intermediates and fine chemicals where optical purity is paramount. Due to its role in facilitating key bond-forming transformations under mild conditions with excellent stereocontrol, it is a staple in both academic research and industrial process chemistry for the production of enantiomerically pure compounds. Its utility extends into the preparation of precursors for advanced materials where specific chirality or functional group manipulation is required.
    Physical Properties

    Melting Point: 136.0-154.7 °C

    mg g kg ml l t