1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE

1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE Basic information
Reaction
Product Name:1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE
Synonyms:BIS[(DI-TERT-BUTYLPHOSPHINO)CYCLOPENTADIENYL]IRON;1,1'-Bis(di-t-butylphosphino)ferrocene,min.98%;1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE;1,1'-Bis(di-tert-butylphosphino)ferrocene,min. 98%;1,1'-Bis(di-tert-butylphosphino)ferrocene ,98%;1,1'-Bis(di-tert-butylphosphin;98% DtBPF;1,1'-Bis(di-tert-butylphosphiNA)ferrocene
CAS:84680-95-5
MF:C26H44FeP210*
MW:474.42
EINECS:626-167-5
Product Categories:Achiral Phosphine;Aryl Phosphine;Classes of Metal Compounds;Fe (Iron) Compounds;Ferrocenes;Metallocenes;Phosphine Ligands;Synthetic Organic Chemistry;Transition Metal Compounds;Catalysis and Inorganic Chemistry;Phosphorus Compounds;Polydentate Phosphine Ligands
Mol File:84680-95-5.mol
1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE Structure
1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE Chemical Properties
Melting point 181-182°C (dec.)
storage temp. Inert atmosphere,Room Temperature
form crystal
color orange to red
Water Solubility Insoluble in water.
InChIKeyFPLSJBJGQLJLSV-UHFFFAOYSA-N
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36/37/39-26
WGK Germany 3
TSCA No
HS Code 29319090
MSDS Information
ProviderLanguage
ALFA English
1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE Usage And Synthesis
Reaction
  1. Ligand for synthesis of polycyclic indoles via Pd-catalyzed intramolecular heteroannulation.
  2. Ligand for the palladium-catalyzed intramolecular arylation of aryl bromides under mild conditions.
  3. Ligand for cross-coupling reactions between bromoarenes and potassium allyltrifluoroborates promoted by a catalyst prepared from Pd(OAc)2 and DTBPF selectively providing γ-coupling products.
  4. Ligand for the copper-catalyzed system for the ß-boration of of a variety of α,ß-unsaturated amides.
  5. Ligand for the synthesis of Paucifloral F and related indanone analogues via palladium-catalyzed α-arylation.
  6. Ligand for the Pd-carbon monoxide complex catalyzed hydroxycarbonylation of aryl halides.
  7. Ligand for the palladium-catalyzed β-C-glycosylation by decarboxylative allylation to normal pyran systems,and cis-2,6-disubstituted tetrahydropyrans.
  8. Pd-catalyzed dearomative indole bisfunctionalization via a diastereoselective arylcyanation.
  9. Ligand for the copper- DTBPF catalyzed C–H activation and carboxylation of terminal alkynes.
Reactions of 84680-95-5_1
Reactions of 84680-95-5_2
Uses1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE is an organophosphine compound and can be used as an organometallic ligand.
UsesThe rate of palladium-catalyzed amination of unactivated aryl chlorides is accelerated by sterically hindered chelating alkyl phosphines, ie, 1,1'-bis(di-tert-butylphosphino)ferrocene.
1,1'-Bis(diphenylphosphino)ferrocene 1,2,3,4,5-PENTAPHENYL-1'-(DI-TERT-BUTYLPHOSPHINO)FERROCENE 1,1'-BIS(DIISOPROPYLPHOSPHINO)FERROCENE 1,1'-BIS(DICYCLOHEXYLPHOSPHINO)FERROCENE 1,1'-Bis (di-t-butylphosphino)ferrocene palladium dichloride, Ferrocene TRIISOPROPYLPHOSPHINE 1,1''-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE PALLADIUM DICHLORI TERT-BUTYLDIISOPROPYLPHOSPHINE 1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE Di-tert-butylphosphine T-BUTYLPHOSPHINE DI-T-BUTYL(I-PROPYL)PHOSPHINE 1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE PALLADIUM DICHLORIDE

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