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| | (S)-(+)-[(S)-2-Diphenylphosphinoferrocenyl] (N,N-dimethylamino) (2-diphenylphosphinophenyl)methane, min. 97% TANIAPHOS Basic information | | Reactions |
| Product Name: | (S)-(+)-[(S)-2-Diphenylphosphinoferrocenyl] (N,N-dimethylamino) (2-diphenylphosphinophenyl)methane, min. 97% TANIAPHOS | | Synonyms: | (S)-(-)-[(S)-2-Diphenylphosphinoferrocenyl](N,N-dimethylamino)(2-
diphenylphosphinophenyl)methane, min. 97% TANIAPHOS;(S)-(-)-[(S)-2-Diphenylphosphinoferrocenyl](N,N-diMethylaMino)(2-diphenylphosphinophenyl)Methane;97% TANIAPHOS;(S)-1-Diphenylphosphino-2-[(S)-a-(N,N-dimethylamino)-o-(diphenylphosphinophenyl)-methyl]ferrocene;(S)-(-)-[(S)-2-Diphenylphosphinoferrocenyl] (N,N-diMethylaMino) (2-diphenylphosphinophenyl)Methane TANIAPHOS;(SP)-1-[(S)-alpha-(DiMethylaMino)-2-(diphenylphosphino)benzyl]-2-diphenylphosphinoferrocene >=97%, optical purity ee: >=99%;Taniaphos SL-T001-2, (2R)-1-[(S)-(Dimethylamino)[2-(diphenylphosphino)phenyl]methyl]-2-(diphenylphosphino)ferrocene (acc to CAS);(S)-(+)-[(S)-2-Diphenylphosphinoferrocenyl] (N,N-dimethylamino) (2-diphenylphosphinophenyl)methane, min. 97% TANIAPHOS | | CAS: | 850444-36-9 | | MF: | C38H34NP2.C5H5.Fe | | MW: | 687.581 | | EINECS: | | | Product Categories: | Chiral Phosphine;Ferrocene Series;Taniaphos Series;metallocene | | Mol File: | 850444-36-9.mol | ![(S)-(+)-[(S)-2-Diphenylphosphinoferrocenyl] (N,N-dimethylamino) (2-diphenylphosphinophenyl)methane, min. 97% TANIAPHOS Structure](CAS/GIF/850444-36-9.gif) |
| | (S)-(+)-[(S)-2-Diphenylphosphinoferrocenyl] (N,N-dimethylamino) (2-diphenylphosphinophenyl)methane, min. 97% TANIAPHOS Chemical Properties |
| alpha | -312° ±15° (c 0.5, CHCl3) | | storage temp. | 2-8°C | | form | Powder | | color | orange | | Stability: | store cold |
| WGK Germany | 3 | | HS Code | 29319090 |
| | (S)-(+)-[(S)-2-Diphenylphosphinoferrocenyl] (N,N-dimethylamino) (2-diphenylphosphinophenyl)methane, min. 97% TANIAPHOS Usage And Synthesis |
| Reactions |
- Ligand for the Ru-catalyzed hydrogenation of $-ketoesters, enamides and itaconates.
- Ligand for Cu-catalyzed asymmetric conjugate addition of Grignard reagents to cyclic enones.
- AgOAc-catalyzed asymmetric amination of glycine Schiff bases with azodicarboxylates.
| | Chemical Properties | Orange powder | | General Description | sold in collaboration with Solvias AG |
| | (S)-(+)-[(S)-2-Diphenylphosphinoferrocenyl] (N,N-dimethylamino) (2-diphenylphosphinophenyl)methane, min. 97% TANIAPHOS Preparation Products And Raw materials |
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