ChemicalBook--->CAS DataBase List--->145214-59-1

145214-59-1

145214-59-1 Structure

145214-59-1 Structure
IdentificationBack Directory
[Name]

(S)-(-)-2,2'-Bis(di-2-furanylphosphino)-6,6'-dimethoxy-1,1'-biphenyl,min.97%
[CAS]

145214-59-1
[Synonyms]

SL-A108-2
(S)-(6,6μ-Dimethoxybiphenyl-2,2μ-diyl)bis(di-2-furylphosphine)
(S)-(-)-2,2'-Bis(di-2-furanylphosphino)-6,6'-dimethoxy-1,1'-biphenyl
(S)-(-)-2,2'-Bis(di-2-furanylphosphino)-6,6'-dimethoxy-1,1'-biphenyl,min.97%
(S)-(-)-2,2''-BIS(DI-2-FURANYLPHOSPHINO)-6,6''-DIMETHOXY-1,1''-BIPHENYL, MIN. 97%
(S)-(6,6'-Dimethoxybiphenyl-2,2'-diyl)bis(di-2-furylphosphine) >=97%, optical purity ee: >=99%
(S)-2-Furyl-MeOBIPHEP, SL-A108-2, (S)-(-)-2,2μ-Bis(di-2-furylphosphino)-6,6μ-dimethoxy-1,1μ-biphenyl
[Molecular Formula]

C30H24O6P2
[MDL Number]

MFCD09753004
[MOL File]

145214-59-1.mol
[Molecular Weight]

542.46
Chemical PropertiesBack Directory
[Boiling point ]

587.5±50.0 °C(Predicted)
[form ]

Powder
[color ]

off-white
[Stability:]

store cold
[CAS DataBase Reference]

145214-59-1
Hazard InformationBack Directory
[Chemical Properties]

White powder
[Uses]

Atropisomeric MeOBIPHEP ligands
[General Description]

sold in collaboration with Solvias AG
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
[WGK Germany ]

3
[HS Code ]

29321900
Questions And AnswerBack Directory
[Reaction]

In many respects the catalytic profile of the MeO-BIPHEP ligands is similar to that of other atropisomeric diphosphines such as binap and its many analogs. The nature of the PR2 group strongly influences the catalytic performance of the metal complexes. The rhodium and ruthenium MeO-BIPHEP catalysts are highly effective for the hydrogenation of various C=O, C=C and C=N bonds and several synthetically useful C-C coupling reactions.
Stereocontrol in palladium-catalyzed propargylic substitutions: kinetc resolution to give enantioenriched 1,5-enynes and propargyl acetates.
Study of enantioselective catalysis of nitroso-Diels-Alder reaction on solid support. Reactions of 145214-59-1
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