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Thianthrene 5,5,10-trioxide

Base Information
  • Chemical Name:Thianthrene 5,5,10-trioxide
  • CAS No.:2362-54-1
  • Molecular Formula:C12H8O3S2
  • Molecular Weight:264.326
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70450179
  • Nikkaji Number:J673.111B
  • Wikidata:Q82269776
Thianthrene 5,5,10-trioxide

Synonyms:Thianthrene 5,5,10-trioxide;2362-54-1;Thianthrene, 5,5,10-trioxide;SCHEMBL11576261;DTXSID70450179

Suppliers and Price of Thianthrene 5,5,10-trioxide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of Thianthrene 5,5,10-trioxide
Chemical Property:
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:0
  • Exact Mass:263.99148646
  • Heavy Atom Count:17
  • Complexity:392
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)S(=O)C3=CC=CC=C3S2(=O)=O
Technology Process of Thianthrene 5,5,10-trioxide

There total 3 articles about Thianthrene 5,5,10-trioxide 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:
Guidance literature:
With bis-[(trifluoroacetoxy)iodo]benzene; In chloroform; at 63 ℃; for 5h;
Guidance literature:
With [bis(acetoxy)iodo]benzene; In chloroform; at 20 ℃; for 24h; Product distribution; Mechanism; other temperatures, other times, different sulphide/oxidizer ratio;
Guidance literature:
With benzyl(triethyl)ammoniumpermanganate; In dichloromethane; Mechanism; other oxidizing agents;
DOI:10.1139/v94-286
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