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ChemicalBook--->CAS DataBase List--->374067-51-3

374067-51-3

374067-51-3 Structure

374067-51-3 Structure
IdentificationBack Directory
[Name]

Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthy]ruthenium(II)
[CAS]

374067-51-3
[Synonyms]

(R)-Ru(OAc)2(H8-BINAP)
Diacetato[(R)-2,2μ-bis(diphenylphosphino)-5,5μ,6,6μ,7,7μ,8,8μ-octahydro-1,1μ-binaphthyl]ruthenium(II)
Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthy]ruthenium(II)
Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl]ruthenium(II),95%
Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(R)-H8-binap]
[Molecular Formula]

C48H46O4P2Ru
[MDL Number]

MFCD09753023
[MOL File]

374067-51-3.mol
[Molecular Weight]

851.91
Chemical PropertiesBack Directory
[Melting point ]

>100°C
[storage temp. ]

2-8°C
[form ]

Powder
[color ]

olive
[Sensitive ]

air sensitive
Safety DataBack Directory
[WGK Germany ]

3
Questions And AnswerBack Directory
[Reaction]

  1. Biaryl bisphosphine ligand. The H8-BINAP ligand, as the ruthenium complex, catalyzes hydrogenation of unsaturated carboxylic acids to a higher ee than does BINAP.
  2. The ruthenium catalyzed hydrogenation of aryl propenoic acid to produce the drug Ibuprofen.
Reactions of 374067-51-3
Hazard InformationBack Directory
[Uses]

(R)-Rutheniumdiacetate-(H8-BINAP) is used as a catalyst in the asymmetric hydrogenation of unsaturated carboxylic acids in supercritical carbon dioxide fluid.
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