双三苯基磷二氯化钯

Bis(triphenylphosphine)palladium(II) chloride

Pd(PPh3)2Cl2 

Bis(triphenylphosphine)palladium(II) dichloride

Buy Pd(PPh3)2Cl2 Buy C36H30Cl2P2Pd Buy CAS 13965-03-2 

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pharmaceutical compounds OLED intermediates palladium catalyst

CAS NO.13965-03-2

Other Names:Palladium(II)bis(triphenylphosphine) dichloride

MF:C36H30Cl2P2Pd

EINECS No.:237-744-2

Place of Origin: Wuhan

Type:Syntheses Material Intermediates

Purity:99.0%min

Brand Name:JDCHEM

Application:Catalyst

Appearance:Yellow crystal

Form:crystal 

Molecular Weight:701.91

M.P.:260℃

B.P.:360 °C at 760 mmHg

Refractive Index:-

Flash Point:181.7 °C

Water solubility:insoluble

COA/MSDS:Available

ISO 9001 manufacturer

Keywords: triphenylphosphine，palladium，Dichlorobis，

Application Guide for Palladium Catalyzed Cross-Coupling Reactions

Bis(triphenylphosphine)palladium(II) dichloride was employed in the following studies:

1. As model catalyst for the evaluation of functionalized silica′s for the adsorptive recovery of homogeneous catalysts, via its interaction with metal centre.

2. As catalyst in the synthesis of diphenylacetylene.

3. One-pot synthesis of furoquinolines, via Pd-catalyzed Sonogashira coupling followed by Cu(I) catalyzed ring closure.

4. Catalyst for Sonogashira coupling of aryl alkynes to 2-bromothiazole and 2-bromothiophene.

General description

Bis(triphenylphosphine)palladium(II) dichloride is an organometallic complex. It is an efficient cross-coupling catalyst for C-C coupling reaction, such as Negishi coupling, Suzuki coupling, Sonogashira coupling and Heck coupling reaction. Detection of bis(triphenylphosphine)palladium(II) dichloride by electrospray ionization quadrupole ion trap mass spectrometry using different imidazolium salts as the charge carrier has been reported. It is employed as catalyst for the Heck reaction medium.

Its worked related to trace metals basis , Asymmetric synthesis, Catalysis or catalyst, Coupling reactions, Cross couplings, Heck Reaction, Ligands,Organic synthesis,Suzuki coupling, Polymer science, Materials Chemistry ,Column chromatography and Organic Compounds , and Arylations, Aminations, Deprotonations, Hydroxylations, Fluorinations