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| | (OXYDI-2,1-PHENYLENE)BIS(DIPHENYLPHOSPHINE) Basic information | | Reaction |
| | (OXYDI-2,1-PHENYLENE)BIS(DIPHENYLPHOSPHINE) Chemical Properties |
| Melting point | 184-187 °C (lit.) | | Boiling point | 608.2±40.0 °C(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Crystalline Powder or Crystals | | color | White to off-white | | BRN | 7729718 | | InChIKey | RYXZOQOZERSHHQ-UHFFFAOYSA-N | | CAS DataBase Reference | 166330-10-5(CAS DataBase Reference) |
| | (OXYDI-2,1-PHENYLENE)BIS(DIPHENYLPHOSPHINE) Usage And Synthesis |
| Reaction |
- Useful as a ligand in the Pd-catalyzed formation of diaryl amines.
- Has been recently applied to the C3 benzylation of indoles.
- Has been recently applied to the monoallylation of ammonia.
- Ligand used in the palladium-catalyzed, aerobic oxidation coupling of acyl chlorides with arylboronic acids.
- Ligand used in carbonylation of aryl iodides.
- Ligand used in the direct C-H arylation of benzothiodiazoles.
- Ligand used in stereo-retentive azacyclization of propargylic carbonates.
- Ligand used in palladium catalyzed benzyne trimerization.
| | Chemical Properties | White to off-white crystalline powder or crystals | | Uses | Ligand for ruthenium-catalyzed greener amine synthesis from amines and alcohols by hydrogen-borrowing.
Ruthenium-Catalyzed N-Alkylation of Amines and Sulfonamides Using Borrowing Hydrogen Methodology | | Uses | suzuki reaction | | General Description | This product has been enhanced for catalytic efficiency. | | reaction suitability | reagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reagent type: ligand
reaction type: Heck Reaction
reagent type: ligand
reaction type: Hydroaminations
reagent type: ligand
reaction type: Negishi Coupling
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling |
| | (OXYDI-2,1-PHENYLENE)BIS(DIPHENYLPHOSPHINE) Preparation Products And Raw materials |
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