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Fluorobenzene is an aryl fluoride and the simplest of the fluorobenzenes, with the formula C 6 H 5 F, often abbreviated PhF. A colorless liquid, it is a precursor to many fluorophenyl compounds. A colorless liquid, it is a precursor to many fluorophenyl compounds.
Fluorobenzenes are a group of aryl fluorides/halobenzenes consisting of one or more fluorine atoms as substituents on a benzene core. They have the formula C 6 H 6–n F n, where n = 1–6 is the number of fluorine atoms.
4,4’-Difluorobenzophenone is prepared by the acylation of fluorobenzene with p-fluorobenzoyl chloride. The conversion is typically conducted in the presence of an aluminium chloride catalyst in a petroleum ether solvent. [1] FC 6 H 4 C(O)Cl + C 6 H 5 F → (FC 6 H 4) 2 CO + HCl
4-Fluorobromobenzene is synthesized via bromination of fluorobenzene in the presence of a Lewis acid catalyst such as iron(III) bromide or aluminium tribromide. [2]4-Bromofluorobenzene is regarded by the Toxic Substances Control Act as a high production volume chemical, that is, a chemical that 1 million pounds (about 500 tonnes) per year is either produced in or imported to the United States.
If the benzene ring contains other substituents, it belongs in Category:Fluorobenzene derivatives. Pages in category "Fluorobenzenes" The following 6 pages are in ...
1,2-Difluorobenzene has been used as solvent for the electrochemical analysis of transition metal complexes. It is relatively chemically inert, weakly coordinating and has a relatively high dielectric constant. In contrast to acetonitrile, DMSO, and DMF it is a weakly coordinating solvent for metal complexes, .
Fluorobenzene derivatives (2 C, 37 P) Fluorobenzenes (7 P) This page was last edited on 1 November 2024, at 15:58 (UTC). Text is available under the Creative Commons ...
The Balz–Schiemann reaction uses tetrafluoroborate and delivers the halide-substituted product, fluorobenzene, which is not obtained by the use of copper fluorides. This reaction displays motifs characteristic of the Sandmeyer reaction.