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Atomfair 2-Fluoro-5-methoxyaniline C7H8FNO
Description 2-Fluoro-5-methoxyaniline (CAS No. 62257-15-2) is a high-purity aromatic amine derivative with the molecular formula C7H8FNO . This compound features a fluorine substituent at the 2-position and a methoxy group at the 5-position of the aniline ring, offering unique reactivity for advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical research, and material science, this reagent is rigorously tested to ensure ??98% purity (HPLC/GC). Available in sealed amber vials or bulk quantities under inert gas to prevent degradation. Store in a cool, dry place away from light and oxidizing agents. Suitable for use in coupling reactions, heterocycle synthesis, and as a…
Description
Description
2-Fluoro-5-methoxyaniline (CAS No. 62257-15-2) is a high-purity aromatic amine derivative with the molecular formula C7H8FNO. This compound features a fluorine substituent at the 2-position and a methoxy group at the 5-position of the aniline ring, offering unique reactivity for advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical research, and material science, this reagent is rigorously tested to ensure ??98% purity (HPLC/GC). Available in sealed amber vials or bulk quantities under inert gas to prevent degradation. Store in a cool, dry place away from light and oxidizing agents. Suitable for use in coupling reactions, heterocycle synthesis, and as a building block for fluorinated compounds.
- CAS No: 62257-15-2
- Molecular Formula: C7H8FNO
- Molecular Weight: 141.14
- Exact Mass: 141.058992041
- Monoisotopic Mass: 141.058992041
- IUPAC Name: 2-fluoro-5-methoxyaniline
- SMILES: COC1=CC(=C(C=C1)F)N
- Synonyms: 2-Fluoro-5-methoxyaniline, 62257-15-2, DTXSID60543842, DTXCID00494627, 694-924-7
Application
2-Fluoro-5-methoxyaniline serves as a versatile intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of kinase inhibitors and antipsychotic agents. Its electron-rich aromatic system facilitates palladium-catalyzed cross-coupling reactions (e.g., Buchwald-Hartwig amination). Researchers utilize this compound to introduce fluorine-methoxy motifs into liquid crystal materials for enhanced dielectric properties. In agrochemistry, it acts as a precursor for herbicides with improved metabolic stability.
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