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Atomfair 2-Fluoro-4-methylaniline C7H8FN

Description 2-Fluoro-4-methylaniline (CAS No. 4870-65-9) is a high-purity aromatic amine compound with the molecular formula C7H8FN . This specialized chemical is an essential intermediate in organic synthesis, featuring a fluorine substituent at the 2-position and a methyl group at the 4-position of the aniline ring. Its unique structure makes it valuable for pharmaceutical, agrochemical, and materials science research. Available in >98% purity (HPLC), this compound is rigorously tested for consistency and stability, ensuring optimal performance in demanding applications. Suitable for use in coupling reactions, heterocycle synthesis, and as a building block for advanced molecular frameworks. Packaged under inert gas to…

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Description

Description

2-Fluoro-4-methylaniline (CAS No. 4870-65-9) is a high-purity aromatic amine compound with the molecular formula C7H8FN. This specialized chemical is an essential intermediate in organic synthesis, featuring a fluorine substituent at the 2-position and a methyl group at the 4-position of the aniline ring. Its unique structure makes it valuable for pharmaceutical, agrochemical, and materials science research. Available in >98% purity (HPLC), this compound is rigorously tested for consistency and stability, ensuring optimal performance in demanding applications. Suitable for use in coupling reactions, heterocycle synthesis, and as a building block for advanced molecular frameworks. Packaged under inert gas to prevent degradation and supplied with comprehensive analytical data (GC/MS, NMR).

  • CAS No: 4870-65-9
  • Molecular Formula: C7H8FN
  • Molecular Weight: 125.14
  • Exact Mass: 125.064077422
  • Monoisotopic Mass: 125.064077422
  • IUPAC Name: 2-fluoro-4-methylaniline
  • SMILES: CC1=CC(=C(C=C1)N)F
  • Synonyms: 2-Fluoro-4-methylaniline, 452-80-2, Benzenamine, 2-fluoro-4-methyl-, NSC 147489, BRN 2637578

Application

2-Fluoro-4-methylaniline serves as a key precursor in the synthesis of fluorinated pharmaceuticals, particularly in the development of kinase inhibitors and antimicrobial agents. Its electron-withdrawing fluorine group enhances reactivity in palladium-catalyzed cross-coupling reactions (e.g., Buchwald-Hartwig amination). The compound is also employed in agrochemical research for creating novel pesticides with improved metabolic stability. Researchers utilize it to modify material properties in conductive polymers and liquid crystal displays (LCDs).

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