CAS 13965-03-2
:Dichlorobis(triphenylphosphine)palladium
- B 1667
- Bis(triphenylphosphine)dichloropalladium
- Bis(triphenylphosphine)dichloropalladium(II)
- Bis(triphenylphosphine)palladium chloride
- Bis(triphenylphosphine)palladium dichloride
- Bis(triphenylphosphine)palladium(II) dichloride
- Bis(triphenylphosphino)-palladium(II) dichloride
- Bis(triphenylphosphino)palladium chloride
- Cis-Bis(Triphenylphosphine)Platinum(Ii) Dichloride
- Dichlorobis(Triphenylphosphine)Palladate (Ii)
- Dichlorobis(Triphenylphosphine)Palladium
- Dichlorobis(triphenylphosphin)palladium
- Dichlorobis(triphenylphosphine)palladium(II)
- Dichlorobis(triphenylphosphine)platinum (II)
- Diclorobis(Trifenilfosfina)Paladio
- Nsc 122924
- Palladium(2+) Chloride-Triphenylphosphane (1:2:2)
- Palladium, dichlorobis(triphenylphosphine)-
- Palladiumbis(triphenylphosphine) dichloride
- Phosphine, Triphenyl-, Palladium(2+) Salt, Dihydrochloride
- Trans-Dichlorobis(triphenyl-phosphine) Palladium(II)
- cis-Bis(triphenylphosphine)platinum(II) chloride
- trans-Bis(triphenylphosphine)palladium dichloride
- See more synonyms
Bis(triphenylphosphine)palladium(II) Dichloride
CAS:Formula:C36H30Cl2P2PdPurity:>98.0%(T)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:701.90Bis(triphenylphosphine)palladium(II) dichloride
CAS:Purity:98%Color and Shape:White to yellow powder or crystalsMolecular weight:701.90trans-Dichlorobis(triphenylphosphine)palladium(II), Pd 14.0% min
CAS:Hydrogenation, hydrosilation, carbonylation, oxidation, and C-C bond formation
Formula:C36H30Cl2P2PdMolecular weight:701.90trans-Dichlorobis(triphenylphosphine)palladium(II), Premion™, 99.95% (metals basis), Pd 14.7% min
CAS:As a catalyst of choice in hydrogenation, hydrosilation, carbonylation, oxidation, elimination, reduction, allyl aceate isomerization, dimerization of 1,3-dienes, and C-C bond formation such as Negishi coupling, Suzuki coupling, Kumada coupling, Sonogashira coupling, Heck coupling and Sonogashira-H
Formula:C36H30Cl2P2PdPurity:99.95%Molecular weight:701.90trans-Dichlorobis(triphenylphosphine)palladium(II), 99% (99.9+%-Pd)
CAS:trans-Dichlorobis(triphenylphosphine)palladium(II), 99% (99.9+%-Pd)
Formula:PdCl2(P(C6H5)3Purity:(99.9+%-Pd)Color and Shape:yellow pwdr.Molecular weight:701.89Dichlorobis(triphenylphosphine)palladium
CAS:Formula:C36H30Cl2P2PdPurity:98%Color and Shape:SolidMolecular weight:701.8969Bis(triphenylphosphine)palladium(II) chloride
CAS:Bis(triphenylphosphine)palladium(II) chlorideFormula:·2C18H15P·Cl2PdPurity:98%Color and Shape: yellow solidMolecular weight:701.89692g/moltrans-Dichlorobis(triphenylphosphine)palladium(II)/potassium phosphate admixture [CatKit single-use vials - 6.32 wt% Pd complex]
CAS:trans-Dichlorobis(triphenylphosphine)palladium(II)/potassium phosphate admixture [CatKit single-use vials - 6.32 wt% Pd complex]
Formula:PdCl2P(C6H5)3K3PO4Color and Shape:off-white pwdr.Molecular weight:701.89Bis(triphenylphosphine)palladium(II)chloride
CAS:Formula:C36H30Cl2P2PdColor and Shape:Yellow to gold crystalline powderMolecular weight:701.91PdCl2(PPh3)2 (HPMC encapsulated)
CAS:Formula:C36H30Cl2P2PdColor and Shape:White to Light yellow to Light orange capsuleMolecular weight:701.90Bis(Triphenylphosphine)palladium (II) chloride
CAS:Formula:C36H30Cl2P2PdPurity:98.0%Color and Shape:Solid, Crystalline Powder or PowderMolecular weight:701.9Bis(triphenylphosphine) palladium(II) chloride, 99.95% (metals basis)
CAS:Formula:(C6H5)3PPdCI2Purity:≥ 99.95%Color and Shape:Pale yellow to brown powder or crystalsMolecular weight:701.89Bis(triphenylphosphine)palladium(II) dichloride
CAS:Bis(triphenylphosphine)palladium(II) dichloride is an organometallic compound that has antibiotic activity. It is the active methylene in a number of drug molecules, including methyldopa, which is used to treat high blood pressure and postural hypotension. Bis(triphenylphosphine)palladium(II) dichloride also has potential use as a target enzyme for cross-coupling reactions. Cross-coupling reactions involve the coupling of organic compounds with organometallic reagents using palladium as a catalyst. The mechanism of this reaction involves the formation of a palladium-carbon bond by oxidative addition and reductive elimination, followed by the release of carbon monoxide. This process leads to the formation of an organometallic compound and an aryl halide. Bis(triphenylphosphine)palladium(II) dichloride can also be used in gel permeation chromFormula:C36H30Cl2P2PdPurity:Min. 95%Color and Shape:Yellow PowderMolecular weight:701.9 g/molDichlorobis(triphenylphosphine) Palladium (II)
CAS:Controlled ProductApplications Dichlorobis(triphenylphosphine) Palladium (II) is used primarily in organometallic catalytic reactions due to the palladium content of the compound. It is also involved in crystalized structures of metallacyclic complexes which show antiinflammatory and antifungal properties.
References Paul, P. et al.: J. Organometal. Chem., 724, 281 (2013); Pandiarajan, D. et al.: J. Organometal. Chem., 708-709, 18, (2012); Shhaheen, F. et al.: J. Organometal. Chem., 693, 315 (2010);Formula:C36H30Cl2P2PdColor and Shape:NeatMolecular weight:701.9









