Description

1-Methoxy-4-(pentafluoro-lambda~6~-sulfanyl)benzene (CAS No. 852469-75-1) is a high-purity fluorinated aromatic compound with the molecular formula C₇H₇F₅OS. This specialized chemical features a pentafluoro-lambda~6~-sulfanyl group attached to a methoxy-substituted benzene ring, offering unique reactivity and stability for advanced synthetic applications. With an IUPAC name of pentafluoro-(4-methoxyphenyl)-lambda6-sulfane, this compound is ideal for researchers working in organofluorine chemistry, materials science, and pharmaceutical development. Our product is rigorously tested to ensure ≥95% purity (GC) and is supplied in sealed glass vials under inert atmosphere to maintain integrity. Suitable for use as a building block in nucleophilic aromatic substitution reactions, ligand synthesis, or as a precursor for functionalized materials with tailored electronic properties.

Properties

• CAS Number: 852469-75-1
• Complexity: 214
• IUPAC Name: pentafluoro-(4-methoxyphenyl)-lambda6-sulfane
• InChI: InChI=1S/C7H7F5OS/c1-13-6-2-4-7(5-3-6)14(8,9,10,11)12/h2-5H,1H3
• InChI Key: HVEWPNYILHLGKS-UHFFFAOYSA-N
• Exact Mass: 234.01377683
• Molecular Formula: C7H7F5OS
• Molecular Weight: 234.19
• SMILES: COC1=CC=C(C=C1)S(F)(F)(F)(F)F
• Topological: 10.2
• Monoisotopic Mass: 234.01377683
• Synonyms: 852469-75-1, DTXSID70732568, 1-Methoxy-4-(pentafluoro-lambda~6~-sulfanyl)benzene, DTXCID00683312, 1-METHOXY-4-(PENTAFLUOROSULFANYL)BENZENE, MFCD16660964, pentafluoro-(4-methoxyphenyl)-lambda6-sulfane, 4-Methoxyphenylsulphur pentafluoride, SCHEMBL1291147, 4-Methoxypentafluorosulfanylbenzene, HVEWPNYILHLGKS-UHFFFAOYSA-N, AKOS016015562, SY358331, 1-methoxy-4-(pentafluorosulfanyl)-benzene, CS-0456351, Pentafluoro(4-methoxyphenyl)-lambda6-sulfane, 1-methoxy-4-(pentafluoro-|E?-sulfanyl)benzene

Application

1-Methoxy-4-(pentafluoro-lambda~6~-sulfanyl)benzene serves as a versatile intermediate in the synthesis of fluorinated liquid crystals and electronic materials due to its strong electron-withdrawing properties. Researchers utilize this compound to develop novel sulfanyl-based ligands for transition metal catalysis in cross-coupling reactions. In medicinal chemistry, it acts as a key precursor for bioactive molecules targeting CNS disorders, leveraging the metabolic stability imparted by the pentafluorosulfanyl group.

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