TRIS[2-(DIPHENYLPHOSPHINO)ETHYL]PHOSPHINE manufacturers
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| | TRIS[2-(DIPHENYLPHOSPHINO)ETHYL]PHOSPHINE Basic information | | Reaction |
| | TRIS[2-(DIPHENYLPHOSPHINO)ETHYL]PHOSPHINE Chemical Properties |
| Melting point | 134-135 °C(lit.) | | Boiling point | 740.1±55.0 °C(Predicted) | | form | Powder | | color | white | | InChIKey | TVLNGWSWPKIYAO-UHFFFAOYSA-N | | SMILES | C(CP(c1ccccc1)c2ccccc2)P(CCP(c3ccccc3)c4ccccc4)CCP(c5ccccc5)c6ccccc6 |
| Hazard Codes | Xn | | Risk Statements | 20/21/22-36/37/38 | | Safety Statements | 26-37/39 | | RIDADR | UN 2811 6.1/PG 3 | | WGK Germany | 3 | | HS Code | 29310099 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Dermal Acute Tox. 4 Inhalation Acute Tox. 4 Oral Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
| | TRIS[2-(DIPHENYLPHOSPHINO)ETHYL]PHOSPHINE Usage And Synthesis |
| Reaction |
- Ligand used in the ruthenium-catalyzed hydrogenation of carbon dioxide facilitated by catalytic quantities of bicarbonate.
- Ligand used in the selective iron-catalyzed transfer hydrogenation of terminal alkynes.
- Ligand used in the selective iron-catalyzed transfer hydrogenation of nitoarenes, without base.
| | Chemical Properties | white to light yellow crystal powde | | Uses | Ligand used in iron-catalyzed, greener reduction of aldehydes to alcohols under transfer hydrogenation conditions.
Fast and selective iron-catalyzed transfer hydrogenations of aldehydes | | General Description | This product has been enhanced for catalytic efficiency. | | reaction suitability | reaction type: Buchwald-Hartwig Cross Coupling Reaction reaction type: Heck Reaction reaction type: Hiyama Coupling reaction type: Negishi Coupling reaction type: Sonogashira Coupling reaction type: Stille Coupling reaction type: Suzuki-Miyaura Coupling reagent type: ligand |
| | TRIS[2-(DIPHENYLPHOSPHINO)ETHYL]PHOSPHINE Preparation Products And Raw materials |
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