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2-Fluoro-3-methoxybenzaldehyde (CAS number 103438-88-6) is a benzaldehyde building block, bearing a fluoride and a methoxy at 2- and 3-positions. 2-Fluoro-3-methoxybenzaldehyde finds widespread use as a precursor for active pharmaceutical ingredients (APIs), particularly in the synthesis of benzosuberone derivatives. To construct benzosuberone cores, 2-fluoro-3-methoxybenzaldehyde reacts with (3-carboxypropyl)triphenylphosphonium bromide through a Wittig reaction. The formation of cycloheptanone ring is achieved through a Friedel-Craft acylation using Eaton's reagent (phosphorus pentoxide and methanesulfonic acid).
2-Fluoro-3-methoxybenzaldehyde is also employed in the synthesis of bicyclic heterocycles, including hydroisoquinolines, acrydinone and quinazolines.
General Information
| CAS Number | 103438-88-6 |
| Chemical Formula | C8H7FO2 |
| Full Name | 2-Fluoro-3-methoxybenzaldehyde |
| Molecular Weight | 154.14 g/mol |
| Synonyms | 2-Fluoro-m-anisaldehyde |
| Classification / Family | Fluorinated building blocks, Benzaldehyde building blocks, Heterocycles, APIs |
Chemical Structure

Product Details
| Purity | 98% |
| Melting Point | Tm = 47 °C – 51 °C |
| Appearance | White crystals |
