15629-92-2

  • Product Name[1,3-Bis(diphenylphosphino)propane]nickel(ii) chloride
  • Molecular FormulaC27H26Cl2NiP2
  • Molecular Weight542
  • Purity99%
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Product Details

Quick Details

  • CasNo: 15629-92-2
  • Molecular Formula: C27H26Cl2NiP2
  • Purity: 99%

Pharmaceutical Grade [1,3-Bis(diphenylphosphino)propane] dichloronickel (II) 15629-92-2 with Best Price

  • Molecular Formula:C27H26Cl2NiP2
  • Molecular Weight:542.04
  • Appearance/Colour:red to red-brown powder or crystals 
  • Vapor Pressure:9E-11mmHg at 25°C 
  • Melting Point:213 °C (dec.)(lit.) 
  • Boiling Point:529.7 °C at 760 mmHg 
  • Flash Point:291.5 °C 
  • PSA:27.18000 
  • LogP:7.02130 

[1,3-Bis(diphenylphosphino)propane]nickel(II) chloride(Cas 15629-92-2) Usage

Description

[1,3-Bis(diphenylphosphino)propane]dichloronickel(II), also known as Ni(dppp)Cl2 or 1,3-Bis(diphenylphosphino)propane nickel(II) chloride, is a versatile organophosphine ligand used extensively in coordination chemistry and catalysis.

Chemical Properties

red to red-brown powder or crystals

Uses

[1,3-Bis(diphenylphosphino)propane]dichloronickel(II) acts as a catalyst in numerous organic reactions, including the Heck reaction, Suzuki-Miyaura coupling, Kumada coupling, and the polymerization of poly(3-alkoxythiophenes). Additionally, it is utilized in the synthesis of block-copolythiophenes, solid-state metathesis polycondensation, and diastereoselective Nozaki-Hiyama-Kishi coupling reactions. The compound is also employed as a precursor for synthesizing metal-fullerene coordination complexes and serves as an effective catalyst in various transformations, such as the N-heterocycle-directed cross-coupling of fluorinated arenes, semihydrogenation of internal alkynes, and borylation of halides and pseudohalides.

InChI:InChI=1/C27H26P2.2ClH.Ni/c1-5-14-24(15-6-1)28(25-16-7-2-8-17-25)22-13-23-29(26-18-9-3-10-19-26)27-20-11-4-12-21-27;;;/h1-12,14-21H,13,22-23H2;2*1H;/q;;;+2/p-2

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