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886059-84-3

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886059-84-3 Structure

886059-84-3 Structure
IdentificationBack Directory
[Name]

DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95%
[CAS]

886059-84-3
[Synonyms]

95% (t-Bu)2(C5H11)PH+BF4-
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
Di-t-butylneopentylphosphoniuM tetrafluoroborate,95% (t-Bu)2(C5H11)PH+BF4-
[Molecular Formula]

C13H30P.BF4
[MDL Number]

MFCD08064039
[MOL File]

886059-84-3.mol
[Molecular Weight]

304.157
Chemical PropertiesBack Directory
[Melting point ]

258-262°C
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

solid
[color ]

white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312-H315-H319-H335
[Precautionary statements ]

P261-P264-P280-P301+P312-P302+P352+P312-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

21/22-36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
Questions And AnswerBack Directory
[Reaction]

  1. 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.
  2. Phosphine used in the palladium-catalyzed, Suzuki cross-coupling reaction.
  3. Phosphine used in the palladium-catalyze Kumada cross-coupling reaction.
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