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Atomfair 1-(4-Fluorophenyl)ethylamine C8H10FN

Description 1-(4-Fluorophenyl)ethylamine (CAS No. 403-40-7) is a high-purity fluorinated organic compound with the molecular formula C8H10FN . This chiral amine is a valuable building block in pharmaceutical and agrochemical research, particularly in the synthesis of enantiomerically pure compounds. Its IUPAC name is 1-(4-fluorophenyl)ethanamine , and it features a fluorinated aromatic ring with an ethylamine substituent, making it useful for structure-activity relationship studies. Our product is rigorously tested for purity and consistency, ensuring optimal performance in synthetic applications. Available in various quantities, it is ideal for medicinal chemistry, asymmetric synthesis, and material science research.

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Description

Description

1-(4-Fluorophenyl)ethylamine (CAS No. 403-40-7) is a high-purity fluorinated organic compound with the molecular formula C8H10FN. This chiral amine is a valuable building block in pharmaceutical and agrochemical research, particularly in the synthesis of enantiomerically pure compounds. Its IUPAC name is 1-(4-fluorophenyl)ethanamine, and it features a fluorinated aromatic ring with an ethylamine substituent, making it useful for structure-activity relationship studies. Our product is rigorously tested for purity and consistency, ensuring optimal performance in synthetic applications. Available in various quantities, it is ideal for medicinal chemistry, asymmetric synthesis, and material science research.

  • CAS No: 403-40-7
  • Molecular Formula: C8H10FN
  • Molecular Weight: 139.17
  • Exact Mass: 139.079727485
  • Monoisotopic Mass: 139.079727485
  • IUPAC Name: 1-(4-fluorophenyl)ethanamine
  • SMILES: CC(C1=CC=C(C=C1)F)N
  • Synonyms: 1-(4-Fluorophenyl)ethylamine, 1-(4-fluorophenyl)ethanamine, 403-40-7, 4-Fluoro-alpha-methylbenzylamine, 1-(4-fluorophenyl)ethan-1-amine

Application

1-(4-Fluorophenyl)ethylamine is widely used as a chiral intermediate in the synthesis of pharmaceuticals, particularly for CNS-active compounds and antidepressants. It serves as a key precursor in asymmetric catalysis and resolution processes. Researchers also employ it in ligand design for transition metal complexes. Its fluorinated aromatic structure enhances binding affinity in drug discovery applications.

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