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18437-78-0

18437-78-0 Structure

18437-78-0 Structure
IdentificationMore
[Name]

TRIS(4-FLUOROPHENYL)PHOSPHINE
[CAS]

18437-78-0
[Synonyms]

TRI(4-FLUOROPHENYL)PHOSPHINE
TRIS(4-FLUOROPHENYL)PHOSPHINE
TRIS(P-FLUOROPHENYL)PHOSPHINE
Phosphine, tris(p-fluorophenyl)-
Tris(p-fluorophenyl)phosphine,99%
Tris(4-fluorophenyl)phosphine 98%
Tris(4-fluorophenyl)phosphine98%
[Molecular Formula]

C18H12F3P
[MDL Number]

MFCD00013553
[Molecular Weight]

316.26
[MOL File]

18437-78-0.mol
Chemical PropertiesBack Directory
[Appearance]

white to light yellow crystal powde
[Melting point ]

79-83 °C(lit.)
[Boiling point ]

160°C/0.1mmHg(lit.)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

Crystalline Powder
[color ]

White to very slightly yellow
[Water Solubility ]

Insoluble in water.
[Sensitive ]

Air Sensitive
[BRN ]

919838
[InChI]

InChI=1S/C18H12F3P/c19-13-1-7-16(8-2-13)22(17-9-3-14(20)4-10-17)18-11-5-15(21)6-12-18/h1-12H
[InChIKey]

GEPJPYNDFSOARB-UHFFFAOYSA-N
[SMILES]

P(C1=CC=C(F)C=C1)(C1=CC=C(F)C=C1)C1=CC=C(F)C=C1
[CAS DataBase Reference]

18437-78-0(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29319090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Chemical Properties]

white to light yellow crystal powde
[Uses]

Tris(4-fluorophenyl)phosphine (TFPP) and tris(2,2,2- trifluoroethyl) phosphite (TTFP) were used as flame-retarding additives in Li-ion battery clectrolytes.
Ligand for rhodium-catalyzed oxygenative addition to terminal alkynes for a greener synthesis esters, amides, and carboxylic acids.
[Preparation]

with 4-bromofluorobenzene, magnesium, and phosphorous (III) trichloride.3 Alternatively, reduction of tris(4-fluorophenyl)phosphine oxide with an iron catalyst.
[General Description]

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
[reaction suitability]

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
[Synthesis]

Tris (4-fluorophenyl)phosphine oxide could be used as a starting material to synthesize Tris(4-fluorophenyl)phosphine. Into the reactor were added 0.2 mmol of tris(4-fluorophenyl)phosphine oxide, 0.36 mmol of trifluoroacetic anhydride, and 1 ml of dioxane as a solvent. Stir at room temperature under a nitrogen atmosphere for 30 min; after the reaction, continue adding 0.2 mmol of sodium bicarbonate, 0.24 mmol of 15-Crown-5, and 1.2 mmol of sodium hydride under a nitrogen environment. Under 150 ℃, stir for 24 hours, stop the reaction, cool to room temperature, and distilled under reduced pressure to remove the solvent. The crude product is separated by column chromatography to obtain Tris(4-fluorophenyl)phosphine with a yield of 74%.
Tris(4-fluorophenyl)phosphine
Spectrum DetailBack Directory
[Spectrum Detail]

Tris(4-fluorophenyl)phosphine(18437-78-0)1HNMR
Tris(4-fluorophenyl)phosphine(18437-78-0)IR
Tris(4-fluorophenyl)phosphine(18437-78-0)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Tris(4-fluorophenyl)phosphine, 99%(18437-78-0)
[Alfa Aesar]

Tris(4-fluorophenyl)phosphine, 98%(18437-78-0)
[Sigma Aldrich]

18437-78-0(sigmaaldrich)
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