1,1 -Bis(diphenylphosphino)ferrocene CAS:12150-46-8

  • Product Name:1,1 -Bis(diphenylphosphino)ferrocene
  • CAS:12150-46-8
  • Molecular formula:C34H28FeP2 10*
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1,1 -Bis(diphenylphosphino)ferrocene CAS:12150-46-8

1,1 -Bis(diphenylphosphino)ferrocene CAS:12150-46-8 Basic information

Product Name: 1,1 -Bis(diphenylphosphino)ferrocene
Synonyms: 1,1 -Bis(diphenylphosphino)ferrocene;1,1 -BIS-(DIPHENYLPHOSPHINO)-FEROCENE;1,1 -Bis(diphenylphosphino) ferrocene, Catalyst Grade;1,1 -Bis(diphenylphosphino)ferrocene, C 73.4%, H 5.2%;1,1μ-Ferrocenebis(diphenylphosphine), 1,1μ-Ferrocenediyl-bis(diphenylp
CAS: 12150-46-8
MF: C34H28FeP2 10*
MW: 554.38
EINECS: 640-119-0
Product Categories: Boron, Nitrile, Thio,& TM-Cpds;Miscellaneous;pharmacetical;Ligand;Catalysts-Ligands;Classes of Metal Compounds;Fe (Iron) Compounds;Ferrocenes;Metallocenes;Phosphine Ligands;Synthetic Organic Chemistry;Transition Metal Compounds;Aromatics;Catalyst;Chelatin
Mol File: 12150-46-8.mol

1,1 -Bis(diphenylphosphino)ferrocene CAS:12150-46-8 Chemical Properties

Melting point: 181-182 °C (dec.)(lit.)
form: crystal
storage temp.: 2-8°C
Water Solubility: Soluble in chloroform, dichloromethane, alcohol and pentane. Insoluble in water.
NIST Chemistry Reference: 1,1 -Bis(diphenylphosphino)ferrocene(12150-46-8)
Stability: Stable. Incompatible with strong oxidizing agents.
Sensitive: Air Sensitive
CAS DataBase Reference: 12150-46-8(CAS DataBase Reference)

Fe

9.7-10.4

10.2

CARBON BY ELEMENTAL ANALYSIS

71.1-76.2

74.2

MELTING POINT(°C)

181-183

182

Purity(%) APPEARANCE

INFRARED SPECTROMETRY

SOLUBILITY IN CHCL3

97-100

YELLOW TO ORANGE POWDER

Conforms to Structure Yellow to orange,clear(2.5%)

99.1


Chemical Properties1,1'-Bis(diphenylphosphino)ferrocene is deep yellow crystalline powder
Usessuzuki reaction
Uses1,1'-Bis(diphenylphosphino)ferrocene used coordination compound in synthesis, readily forms complexes with various metals, i.e. when reacting with the acetonitrile or benzonitrile complexes of PdCl2 it forms (dppf)PdCl2, which i s a popular reagent for palladium-catalyzed coupling reactions.


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