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Atomfair 4,4′-Thiobiphenyl C12H10S2

Description 4,4′-Thiobiphenyl (CAS No. 401-67-2) is a high-purity organic compound with the molecular formula C12H10S2, also known by its IUPAC name 4-(4-sulfanylphenyl)benzenethiol . This aromatic dithiol features a biphenyl core with thiol (-SH) functional groups at the 4 and 4′ positions, making it a valuable building block for organic synthesis and materials science applications. Our product is rigorously tested to ensure exceptional purity and consistency, meeting the stringent requirements of research and industrial applications. It is available in various quantities, packaged under inert conditions to maintain stability. Ideal for use in self-assembled monolayers (SAMs), molecular electronics, and polymer chemistry, this…

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Description

Description

4,4′-Thiobiphenyl (CAS No. 401-67-2) is a high-purity organic compound with the molecular formula C12H10S2, also known by its IUPAC name 4-(4-sulfanylphenyl)benzenethiol. This aromatic dithiol features a biphenyl core with thiol (-SH) functional groups at the 4 and 4′ positions, making it a valuable building block for organic synthesis and materials science applications. Our product is rigorously tested to ensure exceptional purity and consistency, meeting the stringent requirements of research and industrial applications. It is available in various quantities, packaged under inert conditions to maintain stability. Ideal for use in self-assembled monolayers (SAMs), molecular electronics, and polymer chemistry, this compound offers reliable performance for advanced scientific endeavors.

  • CAS No: 401-67-2
  • Molecular Formula: C12H10S2
  • Molecular Weight: 218.3
  • Exact Mass: 218.02239267
  • Monoisotopic Mass: 218.02239267
  • IUPAC Name: 4-(4-sulfanylphenyl)benzenethiol
  • SMILES: C1=CC(=CC=C1C2=CC=C(C=C2)S)S
  • Synonyms: 4,4′-Biphenyldithiol, 6954-27-4, biphenyl-4,4′-dithiol, [1,1′-biphenyl]-4,4′-dithiol, 4,4′-Thiobiphenyl

Application

4,4′-Thiobiphenyl is widely used in the formation of self-assembled monolayers (SAMs) on gold and other metal surfaces, enabling precise surface modifications for sensors and electronic devices. Its bifunctional thiol groups make it a key linker molecule in nanotechnology and molecular electronics, facilitating the construction of conductive molecular junctions. Additionally, it serves as a precursor in polymer chemistry for synthesizing sulfur-containing polymers with tailored properties.

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