Basic information Uses Safety Supplier Related

1,1μ-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride

Basic information Uses Safety Supplier Related

1,1μ-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride Basic information

Product Name:
1,1μ-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride
Synonyms:
  • Dichloro[1,1'-bis(dicyclohexylphosphiNA)ferrocene]palladiuM (II)
  • [1,1′-Bis(di-cyclohexylphosphino)ferrocene]dichloropalladiuM(II)
  • Dichloro[1,1'-bis(dicyclohexylphosphino)ferrocene]palladium (II)
  • PalladiuM, [1,1'-bis(dicyclohexylphosphino-κP)ferrocene]dichloro-, (SP-4-2)-
  • Dichloro [1,1'-bis(dicyclohexy
  • PdCl2(dcypf)
  • Dichloro[1,1'-bis(dicyclohexylphosphino)ferrocene]palladium(II), dichloromethane adduct, 99%
  • 1,1′-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride 98%
CAS:
917511-90-1
MF:
2C17H26P.Cl2Pd.Fe
MW:
755.904
Product Categories:
  • Pd
Mol File:
917511-90-1.mol
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1,1μ-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride Chemical Properties

Melting point:
294-300 °C
storage temp. 
-20°C
form 
Crystalline solid
color 
red-orange microcrystal
InChI
InChI=1S/2C17H26P.2ClH.Fe.Pd/c2*1-3-9-15(10-4-1)18(17-13-7-8-14-17)16-11-5-2-6-12-16;;;;/h2*7-8,13-16H,1-6,9-12H2;2*1H;;/q;;;;;+2/p-2
InChIKey
HRAMBTUEZQOQRK-UHFFFAOYSA-L
SMILES
[CH]1[CH][CH][CH][C]1P(C1CCCCC1)C1CCCCC1.[CH]1[CH][CH][CH][C]1P(C1CCCCC1)C1CCCCC1.[Pd](Cl)Cl.[Fe] |^1:0,1,2,3,4,18,19,20,21,22|
CAS DataBase Reference
917511-90-1
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Safety Information

WGK Germany 
3
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1,1μ-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride Usage And Synthesis

Uses

1,1'-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride is an air-stable catalyst useful in the arylation of various ketones with aryl chlorides and aryl bromides.

Uses

1,1′-Bis(di-cyclohexylphosphino)ferrocene]dichloropalladium(II) or (Pd(dcpf)Cl2) can be used as a catalyst in the synthesis of:

  • α, β-unsaturated amides by hydroaminocarbonylation of alkynes with tertiary amines.
  • Quinazoline derivatives via Suzuki-Miyaura coupling reaction between of quinazolines containing unprotected NH2 group and arylboronic acids.
  • α-aryl carbonyl compounds by α-arylation of ketones with aryl chlorides and aryl bromides.

reaction suitability

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst

1,1μ-Bis(di-cyclohexylphosphino)ferrocene palladium dichlorideSupplier

Shaanxi Rock New Materials Co., Ltd. Gold
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0917-8888777, 3380777,18691786767; 15619786767
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J & K SCIENTIFIC LTD.
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Beijing HwrkChemical Technology Co., Ltd
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Energy Chemical
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021-021-58432009 400-005-6266
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