1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE 18162-48-6,872-50-4,Methylene Chloride,naphthalene,THF,Titanium Dioxide BIS[(DI-TERT-BUTYLPHOSPHINO)CYCLOPENTADIENYL]IRON;1,1'-Bis(di-t-butylphosphino)ferrocene,min.98%;1,1'-BIS(DI-T-BUTYLPHOSPHINO)FERROCENE;1,1'-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE;1,1'-Bis(di-tert-butyl
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-T-BUTYLPHOSPHINO)FERROCENE;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
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
Melting point 181-182°C (dec.)
form crystal
color orange to red
Water Solubility Insoluble in water.
InChIKey FPLSJBJGQLJLSV-UHFFFAOYSA-N
Reaction
Ligand for synthesis of polycyclic indoles via Pd-catalyzed intramolecular heteroannulation.
Ligand for the palladium-catalyzed intramolecular arylation of aryl bromides under mild conditions.
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.
Ligand for the copper-catalyzed system for the ß-boration of of a variety of α,ß-unsaturated amides.
Ligand for the synthesis of Paucifloral F and related indanone analogues via palladium-catalyzed α-arylation.
Ligand for the Pd-carbon monoxide complex catalyzed hydroxycarbonylation of aryl halides.
Ligand for the palladium-catalyzed β-C-glycosylation by decarboxylative allylation to normal pyran systems,and cis-2,6-disubstituted tetrahydropyrans.
Pd-catalyzed dearomative indole bisfunctionalization via a diastereoselective arylcyanation.
Ligand for the copper- DTBPF catalyzed C–H activation and carboxylation of terminal alkynes.
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-T-BUTYLPHOSPHINO)FERROCENE;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
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
Melting point 181-182°C (dec.)
form crystal
color orange to red
Water Solubility Insoluble in water.
InChIKey FPLSJBJGQLJLSV-UHFFFAOYSA-N
Reaction
Ligand for synthesis of polycyclic indoles via Pd-catalyzed intramolecular heteroannulation.
Ligand for the palladium-catalyzed intramolecular arylation of aryl bromides under mild conditions.
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.
Ligand for the copper-catalyzed system for the ß-boration of of a variety of α,ß-unsaturated amides.
Ligand for the synthesis of Paucifloral F and related indanone analogues via palladium-catalyzed α-arylation.
Ligand for the Pd-carbon monoxide complex catalyzed hydroxycarbonylation of aryl halides.
Ligand for the palladium-catalyzed β-C-glycosylation by decarboxylative allylation to normal pyran systems,and cis-2,6-disubstituted tetrahydropyrans.
Pd-catalyzed dearomative indole bisfunctionalization via a diastereoselective arylcyanation.
Ligand for the copper- DTBPF catalyzed C–H activation and carboxylation of terminal alkynes.
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