(SP-4-1)-[1,3-Bis[2,6-bis(1-propylbutyl)phenyl]-4,5-dichloro-1,3-dihydro-2H-imidazol-2-ylidene]dichloro(3-chloropyridine-N)-Palladium, >=98.0%
Others
Properties
| Assay Purity | >=98% |
| Form | Solid |
Safety Information
| Hazard Statement(s) | H315-H319 |
| Precautionary Statement | P264-P280-P337+P313-P305+P351+P338-P302+P352-P332+P313-P362 |
| GHS Pictogram |
|
| Signal word | Warning |
| Storage Temp. | 2-8°C |
Description
Application
It is widely used in BuchwaldHartwig amination reactions for the synthesis of arylamines and heteroarylamines. It is employed in SuzukiMiyaura cross-coupling reactions to form carboncarbon bonds between aryl halides and boronic acids. It can catalyze Sonogashira couplings for the preparation of substituted alkynes.
Purpose
Its primary purpose is to generate an active palladium catalyst that promotes the formation of carboncarbon and carbonheteroatom bonds with high activity selectivity and stability under synthetic reaction conditions.
General Description
It is a palladium(II) complex containing a bulky N-heterocyclic carbene (NHC) ligand two chloride ligands and a coordinated 3-chloropyridine molecule designed as a highly efficient precatalyst for cross-coupling reactions.
Documents
| SDS | |
| COA | |
| Specification | |
| Bulk quote order form | |
| Sample COA |