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158923-11-6

158923-11-6 Structure

158923-11-6 Structure
IdentificationBack Directory
[Name]

(R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE
[CAS]

158923-11-6
[Synonyms]

JOSIPHOS SL-J009-1
(R)-(S)-cy2PF-PtBu2
(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine
(R)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyli-tert-butylphosphine
(R)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-TERT-BUTYLPHOSPHINE
(R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE
(R)-1-[(SP)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-tert-butylphosphine
(R,R)-1-[1-(DI-TERT-BUTYLPHOSPHINO)ETHYL]-2-(DICYCLOHEXYLPHOSPHINO)FERROCENE
(R)-1-[(SP)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-tert-butylphosphine >=97%
(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine,min.97%
(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl] ethyldi-t-butylphosphine, min. 97%
(r,r)-1-[1-(di-tert-butylphosphino)ethyl]-2-(dicyclohexylphosphino)ferrocene (acc to cas)
Ferrocene,1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-,(2R)-
[Molecular Formula]

C32H52FeP2 10*
[MDL Number]

MFCD03426994
[Molecular Weight]

554.55
[MOL File]

158923-11-6.mol
Chemical PropertiesBack Directory
[alpha ]

-185° ±10° (c 0.5, CHCl3)
[form ]

Powder
[color ]

orange
Hazard InformationBack Directory
[Chemical Properties]

Orange powder
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[HS Code ]

29319090
Questions And AnswerBack Directory
[Reaction]

  1. Ligand for Palladium-catalyzed C-N cross-coupling.
  2. Ligand for Palladium-catalyzed C-S cross-coupling.
  3. Ligand for Palladium-catalyzed Kumada couplings of aryl and vinyl tosylates.
  4. Ligand for Rhodium-catalyzed hydroacylation of cyclopropenes, an enatioselective desymmetrization method.
  5. Ligand for Palladium-catalyzed C-O cross-coupling.
  6. Ligand for Rhodium-catalyzed coupling of imidazole derivatives with terminal allenes.
  7. Ligand for Ruthenium-catalyzed C-C coupling of alkynes and alcohols to form branched products of carbonyl allylation


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