Description
1,3,5-Trimethyl-2-(phenylsulfanyl)benzene (CAS No. 33667-80-0) is a high-purity organic compound with the molecular formula C15H16S. This sulfur-containing aromatic derivative is characterized by its unique structural configuration, featuring a phenylsulfanyl group attached to a symmetrically substituted trimethylbenzene ring. Its IUPAC name is 1,3,5-trimethyl-2-phenylsulfanylbenzene, and it is also known by synonyms such as 2,4,6-Trimethyl diphenyl sulfide. This compound is supplied as a research-grade material, rigorously tested for consistency and purity, making it ideal for applications in organic synthesis, materials science, and chemical research. Suitable for use in controlled laboratory environments, it is packaged under inert conditions to ensure stability and longevity.
Properties
- CAS Number: 33667-80-0
- Complexity: 195
- IUPAC Name: 1,3,5-trimethyl-2-phenylsulfanyl-benzene
- InChI: InChI=1S/C15H16S/c1-11-9-12(2)15(13(3)10-11)16-14-7-5-4-6-8-14/h4-10H,1-3H3
- InChI Key: IOVNMGMCDITBSD-UHFFFAOYSA-N
- Exact Mass: 228.09727168
- Molecular Formula: C15H16S
- Molecular Weight: 228.4
- SMILES: CC1=CC(=C(C(=C1)C)SC2=CC=CC=C2)C
- Topological: 25.3
- Monoisotopic Mass: 228.09727168
- Synonyms: 33667-80-0, 1,3,5-TRIMETHYL-2-(PHENYLSULFANYL)BENZENE, DTXSID50495801, DTXCID50446611, 2,4,6-Trimethyl diphenyl sulfide, 1,3,5-trimethyl-2-phenylsulfanylbenzene, mesityl(phenyl)sulfane, 1,3,5-trimethyl-2-(phenylthio)benzene, (2,4,6-trimethyl-phenyl)-phenyl sulfide, 2,4,6-Trimethyldiphenyl sulfide, Phenyl mesityl sulfide, SCHEMBL5887430, AKOS015898772, HS-5654, AC-16459
Application
1,3,5-Trimethyl-2-(phenylsulfanyl)benzene is primarily utilized as a building block in organic synthesis, particularly in the development of sulfur-containing aromatic compounds. Its structural properties make it valuable for studying reaction mechanisms involving sulfur-aryl interactions. Researchers also employ this compound in materials science for investigating novel organic electronic materials. Additionally, it serves as a precursor in the synthesis of ligands for coordination chemistry applications.
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