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ChemicalBook >  Product Catalog >  Organic Chemistry >  Phosphines >  TRICYCLOHEXYLPHOSPHONIUM TETRAFLUOROBORATE

TRICYCLOHEXYLPHOSPHONIUM TETRAFLUOROBORATE

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TRICYCLOHEXYLPHOSPHONIUM TETRAFLUOROBORATE Basic information

Product Name:
TRICYCLOHEXYLPHOSPHONIUM TETRAFLUOROBORATE
Synonyms:
  • Tricyclohexylphosphine tetrafluroborate Pcy3 HBF4
  • Tricyclohexylphosphine tetrafluoroborate IN Stock COA TDS free sample
  • Tricyclohexylphosphine tetrafluoroborate IN Stock MSDS
  • Tricyclohexylphosphine tetrafluoroborate IN Stock free sample and COA
  • Phosphine, tricyclohexyl-, tetrafluoroborate(1-)(1:1)
  • TRICYCLOHEXYLPHOSPHONIUM TETRA
  • TricyclohexylphosphoniuM tetrafluoroborate,Cy3PH+BF4-
  • PCy3.HBF4
CAS:
58656-04-5
MF:
C18H34BF4P
MW:
368.24
EINECS:
672-607-4
Product Categories:
  • Achiral Phosphine
  • Alkyl Phosphine
  • Basic Phosphine LigandsCatalysis and Inorganic Chemistry
  • Catalysis and Inorganic Chemistry
  • organophosphine salt
  • P-BF4
  • Cross-Coupling
  • Phosphine Ligands
  • Phosphorus Compounds
Mol File:
58656-04-5.mol
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TRICYCLOHEXYLPHOSPHONIUM TETRAFLUOROBORATE Chemical Properties

Melting point:
164 °C(lit.)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Dichloromethane (Slightly), Methanol (Slightly)
form 
Powder
color 
White
Water Solubility 
Soluble in water.
InChIKey
KZGFMSRKDNYVKL-UHFFFAOYSA-N
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
22-24/25
RIDADR 
1759
WGK Germany 
3
TSCA 
No
HazardClass 
8
PackingGroup 
III
HS Code 
29209090

MSDS

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TRICYCLOHEXYLPHOSPHONIUM TETRAFLUOROBORATE Usage And Synthesis

Reactions

Non-pyrophoric, air-stable derivative suitable as a replacement for the neat phosphine in a variety of stoichiometric and catalytic processes.

Chemical Properties

White powder

Uses

suzuki reaction

Uses

Tricyclohexylphosphonium Tetrafluoroborate acts as a reagent in the synthesis of potent JAK2 inhibitor BMS-911543 as a potential treatment for myeloproliferative disorders, preparation of Lapatinib intermediate via arylation of furfural with bromochlorofluorobenzyloxyphenylquinazolinamine, structure-activity relationships of carboline and carbazole derivatives as ATP-competitive kinesin spindle protein inhibitors.

Uses

Tricyclohexylphosphine tetrafluoroborate may be used in the following processes:

  • As a ligand for preparing C-homoaporphine alkaloids via microwave-assisted direct-arylation.
  • To synthesize poly-[9,9-bis(3-propylamide-2-methylpropyl sulfonic acid) fluorene]-co-(4,4′-diphenyl) (PFDBSO3H), which can be employed as a template and doping agent for enhancing the conductivity of poly(3,4-ethylenedioxythiophene) (PEDOT) films.
  • To improve the reactivity of palladium-catalyzed Suzuki-Miyaura cross-coupling reaction between MIDA boronates and less activated alkenyl tosylates.

General Description

Tricyclohexylphosphine tetrafluoroborate (PCy3·HBF4) is an inexpensive and air-stable phosphine ligand, commonly used in cross-coupling reactions.

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