Metal Catalysts
Palladium-catalyzed reactions have become increasingly important in the field of organic synthesis. Among the most important are Heck arylations and vinylationas, and cross-coupling reactions such as Suzuki, Stille, Negishi, Sonogashira and aromatic carbon-heteroatom bond-forming procedures. Given below are our products.
| Product Name | CAS # | Formula | M.W. |
| racemic-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl | 98327-87-8 | C44H32P2 | 622.69 |
| 1,1'-bis(diphenylphosphino)ferrocene | 12150-46-8 | C34H28FeP2 | 554.39 |
| [1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) PdCl2(dppf)•CH2Cl2 |
95464-05-4 | C35H30Cl4P2FePd | 816.65 |
| [1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) PdCl2(dppf) |
72287-26-4 | C34H28Cl2FeP2Pd | 731.77 |
| [1,3-Bis(diphenylphosphino)propane]nickel(II) chloride DPPP.NiCl2 |
15629-92-2 | C27H26Cl2NiP2 | 542.05 |
|
[Bis(triphenylphosphine)]dichloroNickel(II) |
14264-16-5 | C36H30Cl2NiP2 | 654.17 |
| Bis(triphenylphosphine)palladium(II)chloride |
13965-03-2 | C36H30Cl2P2Pd | 701.91 |
| Tris(dibenzylideneacetone)dipalladium(0) Pd2(dba)3 |
52409-22-0 51364-51-3 |
C51H42O3Pd2 | 915.73 |
| Bis(dibenzylideneacetone)palladium(0) Pd(dba)2，Pd2(dba)3•dba |
32005-36-0 | C34H28O2Pd | 575.02 |
| 1,3-Bis(2,6-di-i-propylphenyl)imidazolium chloride Ipr.HCl |
250285-32-6 | C27H37ClN2 | 425.05 |
| 1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride Mes.HCl |
141556-45-8 | C21H25ClN2 | 340.89 |
| 1,3-Bis(2,4,6-trimethylphenyl)imidazolinium Chloride |
173035-10-4 | C21H29ClN2 | 344.92 |
| 1,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride |
258278-25-0 | C27H41ClN2 | 429.08 |
| 1,3-Bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazolium tetrafluoroborate |
245679-18-9 | C21H27BF4N2 | 394.26 |
| 1,3-BIS(2,6-DI-ISOPROPYLPHENYL)-4,5-DIHYDROIMIDAZOLIUM TETRAFLUOROBORATE |
282109-83-5 | C27H39N2.BF4 | 478.42 |
| 2-(Dicyclohexylphosphino)-2',4',6'- triisopropylbiphenyl X-PHOS |
564483-18-7 | C33H49P | 476.72 |
Get more infomation about coupling reaction on Wikipedia.