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Atomfair 1-(3-Fluorophenyl)ethanol C8H9FO

Description 1-(3-Fluorophenyl)ethanol (CAS No. 402-63-1) is a high-purity fluorinated aromatic alcohol with the molecular formula C8H9FO. This compound is a valuable intermediate in organic synthesis and pharmaceutical research, featuring a fluorine substituent at the meta position of the phenyl ring and a chiral secondary alcohol group. Its unique structure makes it suitable for asymmetric synthesis, ligand preparation, and as a building block for bioactive molecules. Available in >98% purity (GC), this product is rigorously tested for consistency and stability, ensuring optimal performance in sensitive applications. Packaged under inert gas to prevent degradation, it is ideal for researchers requiring reliable fluorinated…

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Description

Description

1-(3-Fluorophenyl)ethanol (CAS No. 402-63-1) is a high-purity fluorinated aromatic alcohol with the molecular formula C8H9FO. This compound is a valuable intermediate in organic synthesis and pharmaceutical research, featuring a fluorine substituent at the meta position of the phenyl ring and a chiral secondary alcohol group. Its unique structure makes it suitable for asymmetric synthesis, ligand preparation, and as a building block for bioactive molecules. Available in >98% purity (GC), this product is rigorously tested for consistency and stability, ensuring optimal performance in sensitive applications. Packaged under inert gas to prevent degradation, it is ideal for researchers requiring reliable fluorinated synthons.

  • CAS No: 402-63-1
  • Molecular Formula: C8H9FO
  • Molecular Weight: 140.15
  • Exact Mass: 140.063743068
  • Monoisotopic Mass: 140.063743068
  • IUPAC Name: 1-(3-fluorophenyl)ethanol
  • SMILES: CC(C1=CC(=CC=C1)F)O
  • Synonyms: 1-(3-Fluorophenyl)ethanol, 402-63-1, 1-(3-fluorophenyl)ethan-1-ol, 3-Fluoro-alpha-methylbenzyl alcohol, 20044-46-6

Application

1-(3-Fluorophenyl)ethanol is widely used as a chiral precursor in pharmaceutical synthesis, particularly for fluorinated drug candidates. It serves as a key intermediate in the preparation of ligands for asymmetric catalysis and as a building block for agrochemicals. Researchers also employ it in metabolic studies due to its fluorinated aromatic moiety, which mimics natural substrates while offering enhanced stability.

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