{[(Benzenesulfinyl)methyl]sulfanyl}benzene

Base Information

• Chemical Name: {[(Benzenesulfinyl)methyl]sulfanyl}benzene
• CAS No.: 35453-12-4
• Molecular Formula: C13H12OS2
• Molecular Weight: 248.37
• DSSTox Substance ID: DTXSID80508695
• Nikkaji Number: J283.969E
• Mol file: 35453-12-4.mol

Synonyms:35453-12-4;{[(Benzenesulfinyl)methyl]sulfanyl}benzene;phenyl phenylthiomethyl sulfoxide;SCHEMBL11760186;DTXSID80508695;RXUBRXAQZFZKPY-UHFFFAOYSA-N

Chemical Property of {[(Benzenesulfinyl)methyl]sulfanyl}benzene

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 248.03295735
• Heavy Atom Count: 16
• Complexity: 218

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)SCS(=O)C2=CC=CC=C2

Technology Process of {[(Benzenesulfinyl)methyl]sulfanyl}benzene

There total 5 articles about {[(Benzenesulfinyl)methyl]sulfanyl}benzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.6%

bis(phenylthio)methane (3561-67-9) → phenyl phenylthiomethyl sulfoxide (35453-12-4)

Guidance literature:

With dihydrogen peroxide; potassium carbonate; acetic acid; In dichloromethane;

Reference yield: 85.0%

bis(phenylthio)methane (3561-67-9) → phenyl phenylthiomethyl sulfoxide (35453-12-4) + bis(phenylsulfinyl)methane (54888-34-5)

Guidance literature:

With dihydrogen peroxide; methyltrioxorhenium(VII); In ethanol; for 1.5h; Ambient temperature;

DOI:10.1246/bcsj.69.2955

Reference yield:

thiophenol (108-98-5) → phenyl phenylthiomethyl sulfoxide (35453-12-4)

Guidance literature:

Multi-step reaction with 2 steps

1: p-TsOH / benzene / 10 h / Heating

2: H₂O₂ / acetic acid / 2 h / 0 - 20 °C

With dihydrogen peroxide; toluene-4-sulfonic acid; In acetic acid; benzene;

upstream raw materials:

bis(phenylthio)methane

thiophenol

Downstream raw materials:

1-Phenylsulfinyl-1-methylthio-2-(p-chlor-phenyl)-ethylen

S-phenyl 2-phenylethanethioate

S-phenylthiopropionate

S-phenyl 2-hydroxy-2-phenyl(thioethanoate)