Description

Disulfide, bis(3,5-dimethylphenyl) (CAS No. 65151-60-2) is a high-purity organic disulfide compound with the molecular formula C₁₆H₁₈S₂. Also known by its IUPAC name 1-[(3,5-dimethylphenyl)disulfanyl]-3,5-dimethylbenzene, this specialized chemical is widely utilized in research and industrial applications due to its unique structural properties. The compound features two 3,5-dimethylphenyl groups linked by a disulfide bridge, making it valuable for studies in organic synthesis, material science, and polymer chemistry. Our product is rigorously tested to ensure optimal purity and consistency, meeting the stringent requirements of researchers and scientists. Available in various quantities, it is supplied with comprehensive analytical data including GC/MS, NMR, and HPLC for quality assurance.

Properties

• CAS Number: 65151-60-2
• Complexity: 207
• IUPAC Name: 1-[(3,5-dimethylphenyl)disulfanyl]-3,5-dimethyl-benzene
• InChI: InChI=1S/C16H18S2/c1-11-5-12(2)8-15(7-11)17-18-16-9-13(3)6-14(4)10-16/h5-10H,1-4H3
• InChI Key: IRDMKAMOSXNGFZ-UHFFFAOYSA-N
• Exact Mass: 274.08499292
• Molecular Formula: C16H18S2
• Molecular Weight: 274.4
• SMILES: CC1=CC(=CC(=C1)SSC2=CC(=CC(=C2)C)C)C
• Topological: 50.6
• Monoisotopic Mass: 274.08499292
• Synonyms: 3,5-Xylyl disulfide, 65151-60-2, Disulfide, bis(3,5-dimethylphenyl), EINECS 265-540-3, DTXSID7070260, DTXCID4044535, bis(3,5-dimethylphenyl) disulfide, 1-[(3,5-dimethylphenyl)disulfanyl]-3,5-dimethylbenzene, PWU99AJD9C, Di-(3,5-xylyl)disulfide, Di(3,5-xylyl) disulphide, SCHEMBL4032966, bis-(3,5-dimethylphenyl)disulfide, HS-4375, NS00035822

Application

Disulfide, bis(3,5-dimethylphenyl) is commonly employed as a building block in organic synthesis, particularly in the development of sulfur-containing polymers and ligands. It serves as a key intermediate in the preparation of advanced materials, including self-assembled monolayers (SAMs) and metal-organic frameworks (MOFs). Researchers also utilize this compound in studies related to disulfide bond formation and redox chemistry. Its stability and reactivity make it suitable for applications in catalysis and surface modification. Additionally, it finds use in the pharmaceutical and agrochemical industries for the synthesis of novel bioactive molecules.

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