DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95%

DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95%
  • CAS No.:886059-84-3
Other grades of this product :
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
Safety Information
Hazard Codes Xn
Risk Statements 21/22-36/37/38
Safety Statements 26
WGK Germany 3
MSDS Information
DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95% Usage And Synthesis
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.
Uses
  • Cocatalyst for palladium-catalyzed Kumada couplings
DI-T-BUTYLNEOPENTYLPHONIUM TETRAFLUOROBORATE,MIN.95% Preparation Products And Raw materials

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