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Atomfair 2-Fluoro-3-methylaniline C7H8FN

Description 2-Fluoro-3-methylaniline (CAS No. 1978-33-2) is a high-purity fluorinated aromatic amine with the molecular formula C7H8FN . This specialized organic compound is characterized by a fluorine substituent at the ortho position and a methyl group at the meta position relative to the aniline nitrogen. Ideal for pharmaceutical intermediates, agrochemical synthesis, and advanced material research, our product is rigorously tested to ensure ??98% purity (GC) with controlled moisture content. Supplied in amber glass bottles under inert atmosphere to prevent degradation. Key spectral data (HPLC, NMR, MS) available upon request. Hazard classification: Acute Tox. 4 (Oral), Skin Sens. 1.

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Description

Description

2-Fluoro-3-methylaniline (CAS No. 1978-33-2) is a high-purity fluorinated aromatic amine with the molecular formula C7H8FN. This specialized organic compound is characterized by a fluorine substituent at the ortho position and a methyl group at the meta position relative to the aniline nitrogen. Ideal for pharmaceutical intermediates, agrochemical synthesis, and advanced material research, our product is rigorously tested to ensure ??98% purity (GC) with controlled moisture content. Supplied in amber glass bottles under inert atmosphere to prevent degradation. Key spectral data (HPLC, NMR, MS) available upon request. Hazard classification: Acute Tox. 4 (Oral), Skin Sens. 1.

  • CAS No: 1978-33-2
  • Molecular Formula: C7H8FN
  • Molecular Weight: 125.14
  • Exact Mass: 125.064077422
  • Monoisotopic Mass: 125.064077422
  • IUPAC Name: 2-fluoro-3-methylaniline
  • SMILES: CC1=C(C(=CC=C1)N)F
  • Synonyms: 2-Fluoro-3-methylaniline, 1978-33-2, DTXSID00627933, DTXCID30578686, 675-536-7

Application

2-Fluoro-3-methylaniline serves as a key building block in the synthesis of fluorinated active pharmaceutical ingredients (APIs), particularly for kinase inhibitors and CNS-targeting drugs. The compound’s unique substitution pattern enables regioselective coupling reactions in palladium-catalyzed cross-coupling methodologies. Researchers also utilize this aniline derivative in the development of liquid crystal materials and as a precursor for fluorinated dyes with enhanced photostability.

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