(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL

(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL
  • CAS No.:185913-97-7
Other grades of this product :
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL Basic information
Description
Product Name:(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL
Synonyms:(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL;(R)-CL-MEO-BIPHEP;(S)-(-)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL;(S)-CL-MEO-BIPHEP;(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-5,5'-DICHLORO-6,6'-DIMETHOXY-1,1'-BIPHENYL;(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-5,5'-DICHLORO-6,6'-DIMETHOXY-1,1'-BIPHENYL;(-)-5,5'-DICHLORO-2,2'-BIS(DIPHENYLPHOSPHINO)-6,6'-DIMETHOXY-1,1'-BIPHENYL;(+)-5,5'-DICHLORO-2,2'-BIS(DIPHENYLPHOSPHINO)-6,6'-DIMETHOXY-1,1'-BIPHENYL
CAS:185913-97-7
MF:C38H30Cl2O2P2
MW:651.5
EINECS:
Product Categories:Chiral Phosphine;MeOBIPHEP Series
Mol File:185913-97-7.mol
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL Chemical Properties
Melting point 176-180 °C
Boiling point 678.2±55.0 °C(Predicted)
form Powder
color yellow-white
optical activity[α]/D +59±4°, c = 1% in chloroform
Safety Information
Safety Statements 24/25
WGK Germany 3
10-23
MSDS Information
ProviderLanguage
SigmaAldrich English
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL Usage And Synthesis
Description1. Ligand used in the ruthenium catalyzed, enantioselective hydrogenation of alkenes, carbonyls, and imines. 2. Ligand used in the rhodium-catalyzed cyclization of acetylenic aldehydes. 3. Ligand used in the iridium-catalyzed hydrogenative coupling of alkynes to aromatic and aliphatic N-arylsulfonyl aldimines. 4. Asymmetric Cu-catalyzed propargylic substitution with amines,4a and enamines.4b 5. Catalytic desymmetrizing intramolecular Heck reaction. 6. Assembly of 1,3-polyols. 7. Pd-catalyzed diastereo/enantioselective allylic alkylations of ketone enolates. 8. Enantioselective vinylogous Reformatsky-type addition. 9. Cu-catalyzed chemoselective preparation of 2-(pinacolato)boron- substituted allylcopper complexes. and their In situ site-, diastereo-, and enantioselective additions to ketones.
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL Preparation Products And Raw materials

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