Bis[Tris(2-methylphenyl)phosphine]palladium manufacturers
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| Bis[Tris(2-methylphenyl)phosphine]palladium Basic information | Reactions |
Product Name: | Bis[Tris(2-methylphenyl)phosphine]palladium | Synonyms: | Bis[Tris(2-methylphenyl)phosphine]palladium;Bis(tri-o-tolylphosphine)palladiuM(0),98%;Palladium bis(tri-o-tolylphosphine);Bis[tris(2-methylphenyl)phosphine]palladium 97%;Bis(tri-o-tolylphosphine)palladium(0), min. 98%;Bis(tri-o-tolylphosphine)palladiuM(0), Pd 14.9%;Bis(tris(2-tolyl)phosphine)palladium;Bis(tri-o-tolylphosphine) | CAS: | 69861-71-8 | MF: | C42H44P2Pd | MW: | 717.18 | EINECS: | | Product Categories: | Pd;organometallic complex | Mol File: | 69861-71-8.mol | |
| Bis[Tris(2-methylphenyl)phosphine]palladium Chemical Properties |
Melting point | 220-225℃ | storage temp. | -20°C | form | crystal | color | yellow | Water Solubility | Insoluble in water. | Sensitive | Air Sensitive | InChIKey | CUBIJGNGGJBNOC-UHFFFAOYSA-N |
| Bis[Tris(2-methylphenyl)phosphine]palladium Usage And Synthesis |
Reactions | Catalyst used in the palladium-catalyzed amination of aryl and heteroaryl tosylates at room temperature.
| Uses | Bis(tri-o-tolylphosphine)palladium(0) is used as a catalyst for palladium-catalyzed cross-coupling reactions, Kumada coupling and Heck coupling. It is also used in the amination and arylation reactions. | Uses | Catalyst for:
- Palladium-catalyzed cross-coupling reactions and aminations
- Kumada coupling
- Arylation
- Heck coupling
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| Bis[Tris(2-methylphenyl)phosphine]palladium Preparation Products And Raw materials |
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