6-Bromoquinoline,5332-25-2,4-Fluoroindole,387-43-9

3,4-DIAMINOBENZOTRIFLUORIDE 368-71-8 MFCD00042456

2-Cyclopentenone 930-30-3 MFCD00001401

6-Bromoquinoline 5332-25-2 MFCD00024023

4-Fluoro-2-methylbenzonitrile 147754-12-9 MFCD03095106

1-Fluoro-4-iodobenzene 352-34-1 MFCD00001052

Iodobenzene is commercially available, but it may be prepared in the laboratory from aniline via the Sandmeyer reaction. In the first step, the amine functional group is diazotized with hydrochloric acid and sodium nitrite. Potassium iodide is added to the resultant diazonium chloride, causing nitrogen gas to evolve. Any excess nitrite is hydrolyzed with a strong base; the mixture is acidified and the desired product is separated by steam distillation.


4-(Trifluoromethoxy)anisole 710-18-9 MFCD00216942

2,3,4-Trifluorobenzoic acid 61079-72-9 MFCD00061232

3-FLUORO-5-(TRIFLUOROMETHYL)BENZOYL CHLORIDE 171243-30-4 MFCD00061157

4-Fluoroindole 387-43-9 MFCD00055992

1-Chloro-3,4-difluorobenzene 696-02-6 MFCD00042572