Tris[4-(trifluoromethyl)phenyl]phosphine, 98%, Thermo Scientific Chemicals
Tris[4-(trifluoromethyl)phenyl]phosphine, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Tris[4-(trifluoromethyl)phenyl]phosphine, 98%, Thermo Scientific Chemicals

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Quantity:
5 g
1 g
Catalog number A12885.06
also known as A12885-06
Price (USD)/ Each
498.00
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Quantity:
5 g
Request bulk or custom format
Price (USD)/ Each
498.00
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Tris[4-(trifluoromethyl)phenyl]phosphine, 98%, Thermo Scientific Chemicals
Catalog numberA12885.06
Price (USD)/ Each
498.00
-
Add to cart
Chemical Identifiers
CAS13406-29-6
IUPAC Nametris[4-(trifluoromethyl)phenyl]phosphane
Molecular FormulaC21H12F9P
InChI KeyPXYCJKZSCDFXLR-UHFFFAOYSA-N
SMILESFC(F)(F)C1=CC=C(C=C1)P(C1=CC=C(C=C1)C(F)(F)F)C1=CC=C(C=C1)C(F)(F)F
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to yellow
FormCrystals or Crystalline powder
Assay (GC)≥97.5%
Identification (FTIR)Conforms
Melting Point (clear melt)72-76°C
Tris[4-(trifluoromethyl)phenyl]phosphine is a raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Tris[4-(trifluoromethyl)phenyl]phosphine is a raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Kalathil C. Eapen.; Christ Tamborski. The synthesis of tris-(trifluoromethylphenyl)phosphines and phosphine oxides. Journal of Fluorine Chemistry. 1980, 15 (3), 239-243.
  2. Tatsuo Ishiyama.; Hironori Isou.; Takao Kikuchi.; Norio Miyaura. Ortho-C-H borylation of benzoate esters with bis(pinacolato)diboron catalyzed by iridium-phosphine complexes. Chem. Commun. 2010, 46 159-161.