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Atomfair m-Fluorobenzenethiol C6H5FS

Description m-Fluorobenzenethiol (CAS No. 2557-77-9) is a high-purity aromatic thiol compound with the molecular formula C6H5FS and IUPAC name 3-fluorobenzenethiol . This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its reactive thiol (-SH) group and fluorine substitution at the meta position. Our product is rigorously tested to ensure superior quality, with consistent purity levels suitable for sensitive applications. Available in various quantities, it is packaged under inert conditions to maintain stability and prevent oxidation. Ideal for researchers and industrial scientists seeking reliable building blocks for heterocyclic compounds, ligands, or functionalized materials.

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Description

Description

m-Fluorobenzenethiol (CAS No. 2557-77-9) is a high-purity aromatic thiol compound with the molecular formula C6H5FS and IUPAC name 3-fluorobenzenethiol. This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its reactive thiol (-SH) group and fluorine substitution at the meta position. Our product is rigorously tested to ensure superior quality, with consistent purity levels suitable for sensitive applications. Available in various quantities, it is packaged under inert conditions to maintain stability and prevent oxidation. Ideal for researchers and industrial scientists seeking reliable building blocks for heterocyclic compounds, ligands, or functionalized materials.

  • CAS No: 2557-77-9
  • Molecular Formula: C6H5FS
  • Molecular Weight: 128.17
  • Exact Mass: 128.00959950
  • Monoisotopic Mass: 128.00959950
  • IUPAC Name: 3-fluorobenzenethiol
  • SMILES: C1=CC(=CC(=C1)S)F
  • Synonyms: 3-Fluorothiophenol, 2557-77-9, m-Fluorobenzenethiol, EINECS 219-876-2, DTXSID10180261

Application

m-Fluorobenzenethiol serves as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty polymers. Its thiol group enables facile conjugation reactions, while the fluorine moiety enhances metabolic stability in drug design. Researchers employ this compound in catalysis, ligand preparation, and surface modification due to its electron-withdrawing properties. It is also valuable in materials science for creating sulfur-containing frameworks or functionalized surfaces.

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