Identification | Back Directory | [Name]
(R)-(-)-1-[(R)-2-(2'-DIPHENYLPHOSPHINOPHENYL)FERROCENYL]ETHYLDI(BIS-3,5-CF3-PH2)P | [CAS]
387868-06-6 | [Synonyms]
WALPHOS SL-WOO1-1 WALPHOS SL-W001-1 (R)-1-{(R)-2-[2-(Diphenylphosphino)phenyl]-ferrocenyl}ethylbis[3,5-bis-(trifluor (R)-(-)-1-[(R)-2-(2'-DIPHENYLPHOSPHINOPHENYL)FERROCENYL]ETHYLDI(BIS-3,5-CF3-PH2)P (R)-(-)-1-[(R)-2-(2'-Diphenylphosphinophenyl)ferrocenyl]ethyldi(bis-3,5-trifluoromethylphe (R)-(-)-1-[(R)-2-(2'DIPHENYLPHOSPHINOPHENYL)FERROCANYL]ETHYLDI(BIS-3,5-TRIFLUOROMETHYLPHENYL)PHOSPHINE (R)-(-)-1-[(R)-2-(2'-DIPHENYLPHOSPHINOPHENYL)FERROCENYL]ETHYLDI(BIS-3,5-TRIFLUOROMETHYLPHENYL)PHOSPHINE (R)-(-)-1-[(R)-2-(2'-Diphenylphosphinophenyl)ferrocenyl]ethylbis(di-3,5-trifluoroMethylphenyl)phosphine (R)-1-{(RP)-2-[2-(Diphenylphosphino)phenyl]ferrocenyl}ethylbis[3,5-bis-(trifluoromethyl)phenyl]phosphine (r)-1-{(r)-2-[2-(diphenylphosphino)phenyl]-ferrocenyl}ethylbis[3,5-bis-(trifluoromethyl)phenyl]phosphine (R,R)-1-[1-[BIS[3,5-BIS(TRIFLUOROMETHYL)PHENYL]PHOSPHINO]ETHYL]-2-[2-(DIPHENYLPHOSPHINO)PHENYL]FERROCENE (R)-1-[(R)-2-[2-(DIPHENYLPHOSPHINO)PHENYL]-FERROCENYL]ETHYLBIS[3,5-BIS-(TRIFLUOROMETHYL)PHENYL]PHOSPHINE (R)-(-)-1-[(R)-2-(2'-Diphenylphosphinophenyl)ferrocenyl]ethylbis(di-3,5-trifluoromethylphenyl)phosphine,min.97% (R)-(-)-1-[(R)-2-(2'-Diphenylphosphinophenyl)ferrocenyl]ethylbis(di-3,5-trifluoromethylphenyl)phosphine, min. 97% (r,r)-1-{1-[bis[3,5-bis(trifluoromethyl)phenyl]phosphino]ethyl}-2-[2-(diphenylphosphino)phenyl]ferrocene (acc to cas) (R)-1-{(RP)-2-[2-(Diphenylphosphino)phenyl]ferrocenyl}ethylbis[3,5-bis-(trifluoromethyl)phenyl]phosphine,(1S)-1-[(1R)-1-[Bis[3,5-bis(trifluoromethyl)phenyl]phosphino]ethyl]-2-[2-(diphenylphosphino)phe | [Molecular Formula]
C46H32F12FeP2 10* | [MDL Number]
MFCD04112740 | [MOL File]
387868-06-6.mol | [Molecular Weight]
930.52 |
Hazard Information | Back Directory | [Chemical Properties]
Orange powder | [Uses]
Walphos SL-W001-1, in the presence of a ruthenium catalyst may be used as a ligand in the following processes:
- Asymmetric hydrogenation of IPCA-D, a cinnamic acid derivative.
- Addition of 3,5-difluorophenylketimine to 4-methoxyphenylboronic acid to form the corresponding tertiary substituted cyclic sulfamate derivative with high enantioselctivity.2
| [General Description]
The product is an air-stable and non-hygroscopic Solvias chiral phosphine ligand. |
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Energy Chemical
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Sigma-Aldrich
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021-61415566 800-8193336 |
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https://www.sigmaaldrich.cn |
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