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Atomfair Benzene, 1-methyl-2-(phenylthio)- C13H12S
Description 1-Methyl-2-(phenylthio)benzene (CAS No. 13963-35-4) is a high-purity organic sulfur compound with the molecular formula C13H12S . This aromatic thioether features a methyl-substituted benzene ring linked to a phenylthio group, making it a valuable intermediate in synthetic organic chemistry. Its well-defined structure (IUPAC name: 1-methyl-2-phenylsulfanylbenzene ) ensures consistent reactivity for electrophilic substitution and transition metal-catalyzed coupling reactions. Supplied as a clear to pale yellow liquid with >95% purity (GC), this compound is ideal for pharmaceutical research, materials science, and ligand development. Packaged under inert gas in amber glass vials to prevent oxidation, it includes comprehensive analytical data (GC-MS,1H/13C NMR) for…
Description
Description
1-Methyl-2-(phenylthio)benzene (CAS No. 13963-35-4) is a high-purity organic sulfur compound with the molecular formula C13H12S. This aromatic thioether features a methyl-substituted benzene ring linked to a phenylthio group, making it a valuable intermediate in synthetic organic chemistry. Its well-defined structure (IUPAC name: 1-methyl-2-phenylsulfanylbenzene) ensures consistent reactivity for electrophilic substitution and transition metal-catalyzed coupling reactions. Supplied as a clear to pale yellow liquid with >95% purity (GC), this compound is ideal for pharmaceutical research, materials science, and ligand development. Packaged under inert gas in amber glass vials to prevent oxidation, it includes comprehensive analytical data (GC-MS, 1H/13C NMR) for quality verification. Suitable for use in inert atmosphere glove boxes and standard laboratory conditions.
- CAS No: 13963-35-4
- Molecular Formula: C13H12S
- Molecular Weight: 200.30
- Exact Mass: 200.06597156
- Monoisotopic Mass: 200.06597156
- IUPAC Name: 1-methyl-2-phenylsulfanylbenzene
- SMILES: CC1=CC=CC=C1SC2=CC=CC=C2
- Synonyms: 13963-35-4, Benzene, 1-methyl-2-(phenylthio)-, 1-methyl-2-(phenylthio)benzene, DTXSID30161133, DTXCID0083624
Application
This compound serves as a versatile building block in organosulfur chemistry, particularly for synthesizing chiral ligands in asymmetric catalysis. Researchers utilize it to develop photoactive materials due to its electron-rich aromatic system. In medicinal chemistry, it functions as a precursor for biologically active thioether derivatives with potential therapeutic applications. The compound’s stability makes it suitable for studying sulfur-containing polymer systems in materials science.
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