1,3-Bis(diphenylphosphino)propane

1,3-Bis(diphenylphosphino)propane
  • CAS No.:6737-42-4
Other grades of this product :
1,3-Bis(diphenylphosphino)propane Basic information
Product Name:1,3-Bis(diphenylphosphino)propane
Synonyms:1,3-BIS(DIPHENYLPHOSPHINE)PROPANE;1,3-BIS(DIPHENYLPHOSPHINO)PROPANE;DPPP;TRIMETHYLENEBIS(DIPHENYLPHOSPHINE);[3-(Diphenylphosphino)propyl](diphenyl)phosphine;1,3-Propanediylbis(diphenylphosphine);Bis(1,3-diphenylphosphino)propane;Phosphine, 1,3-propanediylbis[diphenyl-
CAS:6737-42-4
MF:C27H26P2
MW:412.45
EINECS:229-791-2
Product Categories:Phosphine Ligands;Synthetic Organic Chemistry;Ligand;API intermediates;organophosphine ligand;API intermediate;Phosphines;Achiral Phosphine;Aryl Phosphine
Mol File:6737-42-4.mol
1,3-Bis(diphenylphosphino)propane Chemical Properties
Melting point 63-65 °C (lit.)
Boiling point 529.7±33.0 °C(Predicted)
Fp 235°C
storage temp. Inert atmosphere,Room Temperature
form Granules or Powder
color White to light yellow-beige
Water Solubility insoluble
Sensitive Air Sensitive
BRN 2821785
InChIKeyLVEYOSJUKRVCCF-UHFFFAOYSA-N
CAS DataBase Reference6737-42-4(CAS DataBase Reference)
NIST Chemistry Reference1,3-Bis(diphenylphosphino)propane(6737-42-4)
EPA Substance Registry SystemPhosphine, 1,3-propanediylbis[diphenyl- (6737-42-4)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-36
WGK Germany 3
10-23
TSCA Yes
HS Code 29310095
MSDS Information
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1,3-Bis(diphenylphosphino)propane English
SigmaAldrich English
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ALFA English
1,3-Bis(diphenylphosphino)propane Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powde
Usessuzuki reaction
Uses1,3-Bis(diphenylphosphino)propane is used as a bidentate ligand in coordination chemistry and form complex dichloro(1,3-bis(diphenylphosphino)propane)nickel by reacting with nickel(II) chloride. This complex is used as a catalyst for Kumada coupling reaction. It also acts as a ligand for palladium(II) catalysts which is useful for the co-polymerization of carbon monoxide and ethylene to get polyketones. Further, it is employed in palladium-catalyzed arylation under Heck reaction and Suzuki reaction. In addition to this, it serves as a catalyst for Negishi coupling and Sonogashira coupling reactions.

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