| Identification | Back Directory | [Name]
1,2,3,4,5-PENTAPHENYL-1'-(DI-TERT-BUTYLPHOSPHINO)FERROCENE | [CAS]
312959-24-3 | [Synonyms]
Q-PHOS
CTC-Q-PHOS
95% CTC-Q-PHOS
1,2,3,4,5-Pentaphenyl-1
Ditert-butyl(cyclopentyl)phosphane
(2,3,4,5-tetraphenylcyclopentyl)benzene
1,2,3,4,5-PENTAPHENYL-1'-(DI-TERT-BUTYL&
1,2,3,4,5-PENTAPHENYL-1-(DI-T-BUTYLPHOSPHINO)FERROCENE
1,2,3,4,5-PENTAPHENYL-1'-(DI-T-BUTYLPHOSPHINO)FERROCENE
1,2,3,4,5-PENTAPHENYL-1'-(DI-TERT-BUTYLPHOSPHINO)FERROCENE
1,2,3,4,5-PENTAPHENYL-1''-(2-TERT-BUTYLPHOSPHINO)FERROCENE
1,2,3,4,5-PENTAPHENYL-1-(DI-T-BUTYLPHOSPHINO)FERROCENE CTC-Q-PHOS
1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene, ctc-q-phos
1,2,3,4,5-PENTAPHENYL-1'-(DI-T-BUTYLPHOSPHINO)FERROCENE, 95% CTC-Q-PHOS
1,2,3,4,5-Pentaphenyl-1'-(di-tert-butylphosphino)ferrocene Application:Heck and Suzuki | [Molecular Formula]
C48H47FeP 10* | [MDL Number]
MFCD03788940 | [MOL File]
312959-24-3.mol | [Molecular Weight]
710.71 |
| Chemical Properties | Back Directory | [Appearance]
Pink solid | [Melting point ]
211-219 °C | [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
Soluble in ether, benzene, toluene and terahydrofuran. | [form ]
Powder | [color ]
pink | [InChIKey]
YOQRDWPCPFCDLP-UHFFFAOYSA-N |
| Hazard Information | Back Directory | [Chemical Properties]
Pink solid | [Uses]
Heck and Suzuki reactions1,2,3,4,5-Pentaphenyl-1'-(di-tert-butylphosphino)ferrocene is a sterically hindered phosphine ligand, which is used in palladium-catalyzed amination, arylation and etherification reactions of aryl chlorides. | [reaction suitability]
reagent type: ligand
reaction type: Arylations
reagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reagent type: ligand
reaction type: Sonogashira Coupling
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling |
| Questions And Answer | Back Directory | [Reaction]
- Ligand used in the preparation of active Pd catalysts for C-C, C-N and C-O bond formation.
- Ligand used in Pd-catalyzed α-arylation of azlactones.
- Pd-catalyzed α-arylation of esters, amides and aldehydes.
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