DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95%
DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95% Basic information
- 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
- Product Categories:
-
- Achiral Phosphine
- Alkyl Phosphine
- organophosphine ligand
- P-H
- Mol File:
- 886059-84-3.mol
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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
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Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 21/22-36/37/38
- Safety Statements
- 26
- WGK Germany
- 3
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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
DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95%Supplier
J & K SCIENTIFIC LTD.
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Energy Chemical
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Shanghai Jian Chao Chemical Technology Co., Ltd.
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