1,1-Bis(diphenylpho...

1,1-Bis(diphenylphosphino)ferrocene

1,1-Bis(diphenylphosphino)ferrocene

Min.Order / FOB Price:Get Latest Price

1 Metric Ton

Negotiable

  • Min.Order :1 Metric Ton
  • Purity: 99.0%
  • Payment Terms : L/C,D/A,D/P,T/T,,MoneyGram,Other

Keywords

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

Quick Details

  • Appearance:deep yellow crystalline powder
  • Application: For Organic Synthesis use
  • PackAge:IN 25kg drums
  • ProductionCapacity:10|Metric Ton|Month
  • Storage:In Room Temperature
  • Transportation: As Per MSDS

Superiority:

Product Name: 1,1'-Bis(diphenylphosphino)ferrocene
Synonyms: DPPF;1,1'-BIS(DIPHENYLPHOSPHINO)FERROCENE;1,1'-FERROCENEDIYL-BIS(DIPHENYLPHOSPHINE);1,1'-FERROCENEBIS(DIPHENYLPHOSPHINE);1,1'-bis(diphenyphosphino)ferrocene;1,1'-bis(diphenyphosphino)ferrocene(dppf);1,1'-BIS(DIPHENYLPHOSPHINO)FERROCENE, 97 %;1,1'-Bis(diphenylphosphino)ferrocene,99%DPPF
CAS: 12150-46-8
MF: C34H28FeP2 10*
MW: 554.38
EINECS: 430-420-3
Product Categories: Phosphines;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;Chelating Agents & Ligands;Pharmaceutical intermediates
Mol File: 12150-46-8.mol
1,1'-Bis(diphenylphosphino)ferrocene Structure

 

Details:

1,1'-Bis(diphenylphosphino)ferrocene Chemical Properties
mp  181-182 °C (dec.)(lit.)
storage temp.  2-8°C
Sensitive  Air Sensitive
Stability: Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference 12150-46-8(CAS DataBase Reference)
NIST Chemistry Reference 1,1'-Bis(diphenylphosphino)ferrocene(12150-46-8)
Chemical Properties deep yellow crystalline powder
Usage suzuki reaction
Usage Commonly 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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