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ChemicalBook--->CAS DataBase List--->185913-98-8

185913-98-8

185913-98-8 Structure

185913-98-8 Structure
IdentificationBack Directory
[Name]

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

185913-98-8
[Synonyms]

(R)-CL-MEO-BIPHEP
(S)-CL-MEO-BIPHEP
min.(s)-cl-meo-biphep
(5,5'-Dichloro-6,6'-dimethoxy-2,2'-biphenyldiyl)bis(diphenylphosphine)
(-)-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
(R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL
(r)-(-)-5,5'-dichloro-2,2'-bis(diphenylphosphino)-6,6'-dimethoxy-1,1'-biphenyl
(S)-(-)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL
(-)-(5,5'-DICHLORO-6,6'-DIMETHOXY-1,1'-BIPHENYL)-2,2'-DIYL-BIS(DIPHENYLPHOSPHINE)
(+)-(5,5'-DICHLORO-6,6'-DIMETHOXY-1,1'-BIPHENYL)-2,2'-DIYL-BIS(DIPHENYLPHOSPHINE)
(S)-(-)-5,5'-Dichloro-6,6'-diMethoxy-2,2'-bis(diphenylphosphino)-1,1'-biphenyl (S)-Cl-MeO-BIPHEP
(S)-(-)-5,5'-Dichloro-6,6'-dimethoxy-2,2'-bis(diphenylphosphino)-1,1'-biphenyl,min.95%(S)-Cl-MeO-BIPHEP
[Molecular Formula]

C38H30Cl2O2P2
[MDL Number]

MFCD03426987
[MOL File]

185913-98-8.mol
[Molecular Weight]

651.5
Chemical PropertiesBack Directory
[Melting point ]

176-180 °C
[Boiling point ]

678.2±55.0 °C(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

Powder
[color ]

yellow-white
[optical activity]

[α]20/D 59.0±4°, c = 1% in chloroform
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[F ]

10-23
Questions And AnswerBack Directory
[Reactions]

  1. 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.
Reactions of 185913-98-8
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