1,2-BIS(DIPHENYLPHOSPHINO)BENZENE CAS 13991-08-7
Introduction:Basic information about 1,2-BIS(DIPHENYLPHOSPHINO)BENZENE CAS 13991-08-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
1,2-BIS(DIPHENYLPHOSPHINO)BENZENE Basic information
| Product Name: | 1,2-BIS(DIPHENYLPHOSPHINO)BENZENE |
| Synonyms: | 1,2-BIS(DIPHENYLPHOSPHINO)BENZENE;1,2-BIS(DIPHENYLPHOSPHINO)BENZENE 98%;1,2-Bis(diphenylphosphanyl)benzene;dppbe;dppben;dppbenz;dppBz;o-bis(diphenylphosphino)benzene |
| CAS: | 13991-08-7 |
| MF: | C30H24P2 |
| MW: | 446.47 |
| EINECS: | |
| Product Categories: | Achiral Phosphine;Aryl Phosphine;Ligand;Catalysis and Inorganic Chemistry;Phosphorus Compounds;Polydentate Phosphine Ligands;organophosphine ligand |
| Mol File: | 13991-08-7.mol |
1,2-BIS(DIPHENYLPHOSPHINO)BENZENE Chemical Properties
| Melting point | 183-188 °C (lit.) |
| Boiling point | 546.9±33.0 °C(Predicted) |
| storage temp. | Inert atmosphere,Room Temperature |
| form | Fine Crystalline Powder |
| color | White |
| Water Solubility | Insoluble in water. |
| Sensitive | Air Sensitive |
| InChI | InChI=1S/C30H24P2/c1-5-15-25(16-6-1)31(26-17-7-2-8-18-26)29-23-13-14-24-30(29)32(27-19-9-3-10-20-27)28-21-11-4-12-22-28/h1-24H |
| InChIKey | NFRYVRNCDXULEX-UHFFFAOYSA-N |
| SMILES | P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1P(C1C=CC=CC=1)C1C=CC=CC=1 |
| CAS DataBase Reference | 13991-08-7(CAS DataBase Reference) |
Safety Information
| Risk Statements | 36/37/38 |
| Safety Statements | 24/25 |
| WGK Germany | 3 |
| TSCA | No |
| HS Code | 29319090 |
| Storage Class | 11 - Combustible Solids |
| Chemical Properties | white to light yellow crystal powde |
| Uses | 1,2-Bis(diphenylphosphino)benzene (DPPB) can be used:
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| Application | 1,2-Bis(diphenylphosphino)benzene is a highly efficient bidentate phosphine ligand. It forms a stable five-membered ring chelate with a single transition metal atom (such as palladium, nickel, rhodium, gold, etc.) through its two adjacent diphenylphosphine groups. This structure gives the catalyst high activity and high stability, so it is widely used in various homogeneous catalytic reactions. |
| reaction suitability | reagent type: ligand reaction type: Baeyer-Villiger Oxidation reagent type: ligand reaction type: Cycloadditions reagent type: ligand reaction type: Reductions |
