![[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)](/uploads/files/global/products/chemical-biology/MND-54646-47592.png "[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)")
![[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)](/uploads/files/global/products/chemical-biology/.webimages/MND-54738-47674.jpeg "[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)")
[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) / 1 G
Safety Information
Hazard Statements
Precautionary Statements
Pictograms
Properties
| Flash Point (C) | Not available |
| Flash Point (F) | Not available |
| Melting Point | 266-283 °C (lit.) |
Product Description
[1,1′-BIS(DIPHENYLPHOSPHINO)FERROCENE]DICHLOROPALLADIUM(II) is a coordination compound widely used in organic synthesis. With its unique structure, it serves as an efficient catalyst in various cross-coupling reactions, facilitating the formation of complex organic molecules.
Application:
This compound is instrumental in catalyzing cross-coupling reactions, playing a crucial role in organic synthesis. It finds application in the construction of diverse molecular structures in the field of chemical research and development.
Articles:
- [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium/1,1′-Bis(diphenylphosphino)ferrocene Catalyzed Synthesis of 2,3-Diamino-1,4-naphthoquinones
Publication Date: 12 March 2007 (online)
Xiao Lei Wang, Xiu Fang Zheng, Lei Wang, John Reiner, Wei Lin Xie, Jun Biao Chang
https://doi.org/10.1055/s-2007-965983
- Rearrangement products in aqueous photolysis of thifensulfuron methyl
Publication Date: Available online 20 June 2017
Ashok K. Sharma, David L. Ryan, Nina L. Marr, Michael P. Wadsley, Steve F. Cheatham
https://doi.org/10.1016/j.jphotochem.2017.06.028
- Steric and electronic interactions between cofacial metallocene rings
Publication Date: June 1, 1988
Regina Arnold, Bruce M. Foxman, Myron Rosenblum, and William B. Euler