2,4,5-Trifluorobenzonitrile was used in preparation of novel linker in solid phase synthesis, 2-(2-fluoro-4-hydroxymethyl-5-methoxy-phenoxy)acetic acid.
2,4,5-Trifluorobenzonitrile can be used as pairs of pseudopure states for 4- and 5-qubit NMR systems.
2,4,5-Trifluorobenzonitrile serves as a building block for introducing a fluorinated benzonitrile segment to the target molecule by nucleophilic aromatic substitution. A fluorinated analog of platensimycin, an antibiotic, can be readily synthesized from 2,4,5-trifluorobenzonitrile.
Raman and FTIR spectra of 2,4,5- Trifluorobenzonitrile was studied. Highly regioselective substitution reaction of 2,4,5-trifluorobenzonitrile was reported.
