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| DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95% Basic information | | Reaction |
| Product Name: | DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95% | | Synonyms: | ditert-butyl(2,2-dimethylpropyl)phosphanium,tetrafluoroborate;DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95%;Di-t-butylneopentylphosphoniumtetrafluoroborate,min.95%;Di-t-butylneopentylphosphonium tetrafluoroborate, min. 95%;Bis(1,1-dimethylethyl)(2,2-dimethylpropyl)phosphine tetrafluoroborate;95% (t-Bu)2(C5H11)PH+BF4-;DI-T-BUTYLNEOPENTYLPHOSPHONIUM TETRAFLUOROBORATE,(T-BU)2(C5H11)PH+BF4-;Di-t-butylneopentylphosphoniuM tetrafluoroborate,95% (t-Bu)2(C5H11)PH+BF4- | | CAS: | 886059-84-3 | | MF: | C13H30BF4P | | MW: | 304.16 | | EINECS: | | Product Categories: | Achiral Phosphine;Alkyl Phosphine;organophosphine ligand;P-H | | Mol File: | 886059-84-3.mol |
| DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95% Chemical Properties |
| Melting point | 258-262°C | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | form | solid | | color | white |
| DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95% Usage And Synthesis |
| Reaction |
- The phosphine, used in combination with a palladium source and base, produces a highly effective catalyst for the Buchwald- Hartwig amination of aryl bromides at room temperature.
- Phosphine used in the palladium-catalyzed, Suzuki cross-coupling reaction.
- Phosphine used in the palladium-catalyze Kumada cross-coupling reaction.
| | Uses | - Cocatalyst for palladium-catalyzed Kumada couplings
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| DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95% Preparation Products And Raw materials |
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