185913-97-7 Usage
Uses
Used in the Chemical Industry:
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL is used as a ligand for the ruthenium-catalyzed, enantioselective hydrogenation of alkenes, carbonyls, and imines. This application is significant for producing chiral molecules with high enantiomeric purity, which are essential in the pharmaceutical and agrochemical industries.
Used in the Pharmaceutical Industry:
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL is used as a ligand in the rhodium-catalyzed cyclization of acetylenic aldehydes. This reaction is important for the synthesis of complex molecular structures, which can be further utilized in the development of novel pharmaceutical compounds.
Used in the Synthesis of Complex Molecules:
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL is used as a ligand in the iridium-catalyzed hydrogenative coupling of alkynes to aromatic and aliphatic N-arylsulfonyl aldimines. This reaction allows for the formation of complex molecular structures with potential applications in various fields, including materials science and pharmaceuticals.
Used in Asymmetric Catalysis:
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL is used as a ligand in asymmetric Cu-catalyzed propargylic substitution with amines and enamines. This reaction is crucial for the synthesis of chiral molecules with potential applications in the pharmaceutical and agrochemical industries.
Used in the Preparation of 1,3-Polyols:
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL is used as a ligand in the assembly of 1,3-polyols. These polyols are important building blocks in the synthesis of various biologically active compounds and materials.
Used in Pd-Catalyzed Allylic Alkylations:
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL is used as a ligand in Pd-catalyzed diastereo/enantioselective allylic alkylations of ketone enolates. This reaction is essential for the synthesis of chiral molecules with potential applications in the pharmaceutical and agrochemical industries.
Used in Enantioselective Vinylogous Reformatsky-Type Addition:
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL is used as a ligand in the enantioselective vinylogous Reformatsky-type addition. This reaction is important for the synthesis of chiral β-hydroxy esters, which are valuable intermediates in the preparation of various biologically active compounds.
Used in Cu-Catalyzed Preparation of Allylcopper Complexes:
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-
Check Digit Verification of cas no
The CAS Registry Mumber 185913-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,9,1 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 185913-97:
(8*1)+(7*8)+(6*5)+(5*9)+(4*1)+(3*3)+(2*9)+(1*7)=177
177 % 10 = 7
So 185913-97-7 is a valid CAS Registry Number.
185913-97-7Relevant articles and documents
Process for the preparation of enantiomerically pure (5,5'-dichloro-6,6'-dimethoxy-biphenyl-2,2'-diyl)- bis(diphenylphosphine oxides)
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, (2008/06/13)
The invention relates to the preparation of enantiomerically pure bis-diphenylphosphine oxides in a particularly advantageous manner by (1) reacting an aromatic bromine compound with a diphenylphosphinic chloride in a mixture of tetrahydrofuran and an aro
Process for preparing oprtically active trimethyllactic acid and its ester
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, (2008/06/13)
The invention relates to a novel process for preparing optically active trimethyllactic acid and/or its esters by catalytic hydrogenation of trimethylpyruvic acid and/or its esters in the presence of noble metal complex catalysts containing phosphorus ligands.
Diphosphines
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, (2008/06/13)
The invention relates to the preparation and use as catalysts of diphosphines of the formula (I) in which R is C6-C14-aryl or C4-C13-heteroaryl containing 1 to 3 heteroatoms selected from the group consisting of