Atomfair Methylphenylsulfide Thioanisole C7H8S

Description Methylphenylsulfide (Thioanisole) is a high-purity organosulfur compound with the molecular formula C7H8S and CAS number 100-68-5 . This colorless to pale yellow liquid is widely utilized in organic synthesis, pharmaceuticals, and material science due to its role as a versatile building block. With a boiling point of approximately 188??C and a distinct aromatic odor, Methylphenylsulfide is soluble in organic solvents such as ethanol, ether, and acetone but insoluble in water. Its IUPAC name, methylsulfanylbenzene , reflects its structure??a benzene ring substituted with a methylthio group. Ideal for researchers and industrial applications, our product is rigorously tested to ensure ??98%…

Description

Description

Methylphenylsulfide (Thioanisole) is a high-purity organosulfur compound with the molecular formula C7H8S and CAS number 100-68-5. This colorless to pale yellow liquid is widely utilized in organic synthesis, pharmaceuticals, and material science due to its role as a versatile building block. With a boiling point of approximately 188??C and a distinct aromatic odor, Methylphenylsulfide is soluble in organic solvents such as ethanol, ether, and acetone but insoluble in water. Its IUPAC name, methylsulfanylbenzene, reflects its structure??a benzene ring substituted with a methylthio group. Ideal for researchers and industrial applications, our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed containers to maintain stability. Synonyms include Thioanisole, Methyl phenyl sulfide, and Benzene, (methylthio)-.

  • CAS No: 100-68-5
  • Molecular Formula: C7H8S
  • Molecular Weight: 124.21
  • Exact Mass: 124.03467143
  • Monoisotopic Mass: 124.03467143
  • IUPAC Name: methylsulfanylbenzene
  • SMILES: CSC1=CC=CC=C1
  • Synonyms: Thioanisole, 100-68-5, Methyl phenyl sulfide, Benzene, (methylthio)-, Thioanisol

Application

Methylphenylsulfide is a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fragrances. It serves as a precursor for sulfoxide and sulfone derivatives, which are critical in asymmetric synthesis and catalysis. Researchers also employ it as a ligand in transition-metal complexes and as a sulfur source in organic transformations. Its stability and reactivity make it valuable in the development of novel materials and fine chemicals.

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