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Tris(4-fluorophenyl)phosphine
Catalog Number
ACM18437780
Product Name
Tris(4-fluorophenyl)phosphine
Structure
![{[CurrentData.Name]}](https://resource.alfachemic.com/structure/18437-78-0.gif)
CAS
18437-78-0
Synonyms
Phosphine, Tris(4-Fluorophenyl)-
IUPAC Name
tris(4-fluorophenyl)phosphane;
Molecular Weight
316.26
Molecular Formula
C18H12F3P
Canonical SMILES
C1=CC(=CC=C1F)P(C2=CC=C(C=C2)F)C3=CC=C(C=C3)F;
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;
InChI Key
GEPJPYNDFSOARB-UHFFFAOYSA-N;
Purity
97%
Appearance
Grey white solid
Complexity
275
Covalently-Bonded Unit Count
1
Exact Mass
316.063g/mol
H-Bond Acceptor
3
Heavy Atom Count
22
Monoisotopic Mass
316.063g/mol
NSC Number
158458
Rotatable Bond Count
3
Topological Polar Surface Area
0A^2
Application
Tris(4-fluorophenyl)phosphine serves as a versatile and innovative component, primarily utilized as a ligand for rhodium-catalyzed oxygenative addition to terminal alkynes, facilitating the environmentally friendly synthesis of esters, amides, and carboxylic acids. This product not only plays a critical role in organic synthesis but is also prominent in the development of pharmaceuticals, agrochemicals, and dyes. Beyond its synthetic applications, it acts as a flame-retarding additive in lithium-ion battery electrolytes. Aligned with our commitment to greener chemistry, Tris(4-fluorophenyl)phosphine adheres to the principles of sustainable chemistry and has been optimized for catalytic efficiency, demonstrating our dedication to sustainability and innovation.
February 28, 2025
Essential Reagent for Greener Research
Tris(4-fluorophenyl)phosphine is excellent in rhodium-catalyzed synthesis. Its effectiveness in producing esters and amides enhanced our research efficiency considerably. A reliable choice for sustainable chemistry efforts.
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