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| 4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE Basic information | Reactions |
Product Name: | 4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE | Synonyms: | 4,6-Bis(diphenylphosphino)phenoxazine 97%;N-XantPhos 97%;4,6-Bis(diphenylphosphino)phenoxazine, min. 98%;4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE;4,6-Bis(diphenylphosphino)phenoxazine, NIXANTPHOS;4,6-Bis(diphenylphosphino)phenoxazine,min.98%NIXANTPHOS;4,6-Bis(diphenylphosphino)phenoxazine, 98+%;4,6-Bis(diphenylphosphino)phenoxazine, 98+% NIXANTPHOS | CAS: | 261733-18-0 | MF: | C36H27NOP2 | MW: | 551.55 | EINECS: | | Product Categories: | Achiral Phosphine;Aryl Phosphine;Phosphine Ligands;Synthetic Organic Chemistry;organophosphine ligand | Mol File: | 261733-18-0.mol | |
| 4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE Chemical Properties |
Melting point | 256-262 °C | Boiling point | 662.1±55.0 °C(Predicted) | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | pka | 1.34±0.20(Predicted) | form | Powder | color | white to off-white | Water Solubility | Miscible with water. | InChIKey | HSWZLYXRAOXOLL-UHFFFAOYSA-N | CAS DataBase Reference | 261733-18-0 |
Risk Statements | 36/37/38 | Safety Statements | 22-24/25 | WGK Germany | 3 | TSCA | No | HS Code | 2934.99.4400 |
| 4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE Usage And Synthesis |
Reactions |
- A large bite-angle chelating bisphosphine that provides high levels of linear-to-branched selectivity in the hydroformylation of alkenes.
- A Deprotonatable Ligand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides.
| Uses | 4,6-Bis(diphenylphosphino)phenoxazine used as an intermediate in the manufacture of pharmaceuticals, agrochemicals, dyestuffs, fine chemicals, medical and material synthesis. | Uses | 4,6-Bis(Diphenylphosphino)phenoxazine is used as a palladium catalyst in reactions involving the synthesis of triarylmethanes. | Uses | N-XantPhos is a deprotonatable chelating aryldiphosphine ligand that can be used in:
- The preparation of Pd-NiXantphos catalyst system for the room temperature cross-coupling reactions of unactivated aryl chlorides.
- The synthesis of cinchonine iridium(III) cyclometalated complex that exhibits luminescence and good quantum efficiency.
- N-XantPhos and N-modified counterparts are also used in the preparation of rhodium based catalysts for hydroformylation reaction.
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| 4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE Preparation Products And Raw materials |
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