Benzene, 1,3,5-tris(phenylsulfonyl)-

Base Information

Chemical Name:Benzene, 1,3,5-tris(phenylsulfonyl)-
CAS No.:6461-84-3
Molecular Formula:C₂₄H₁₈O₆S₃
Molecular Weight:498.601
Hs Code.:
DSSTox Substance ID:DTXSID30452391
Wikidata:Q82273003

Synonyms:Benzene, 1,3,5-tris(phenylsulfonyl)-;6461-84-3;SCHEMBL1332008;DTXSID30452391;1,3,5-tris(phenylsulfonyl)benzene

Suppliers and Price of Benzene, 1,3,5-tris(phenylsulfonyl)-

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 Benzene, 1,3,5-tris(phenylsulfonyl)-

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:498.02655181
Heavy Atom Count:33
Complexity:810

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)S(=O)(=O)C2=CC(=CC(=C2)S(=O)(=O)C3=CC=CC=C3)S(=O)(=O)C4=CC=CC=C4

Technology Process of Benzene, 1,3,5-tris(phenylsulfonyl)-

There total 6 articles about Benzene, 1,3,5-tris(phenylsulfonyl)- 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: 68.0%

: 546834-93-9
1-phenylthio-3,5-bis(phenylsulfonyl)benzene

: 6461-84-3
1,3,5-tris(phenylsulfonyl)benzene

Guidance literature:: With dihydrogen peroxide; In acetic acid; for 0.5h; Heating;
DOI:10.1023/A:1022563529344

Reference yield:

: 108-98-5
thiophenol

: 6461-84-3
1,3,5-tris(phenylsulfonyl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / 1-methyl-pyrrolidin-2-one / 0.5 h / 50 °C

2: 68 percent / 35 percent H₂O₂ / acetic acid / 0.5 h / Heating

With dihydrogen peroxide; potassium carbonate; In 1-methyl-pyrrolidin-2-one; acetic acid;
DOI:10.1023/A:1022563529344

Reference yield:

: 546834-88-2
3-nitro-5-phenylthiodiphenyl sulfone

: 6461-84-3
1,3,5-tris(phenylsulfonyl)benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / 35 percent H₂O₂ / acetic acid / 1 h / Heating

2: 73 percent / K₂CO₃ / 1-methyl-pyrrolidin-2-one / 0.5 h / 50 °C

3: 68 percent / 35 percent H₂O₂ / acetic acid / 0.5 h / Heating

With dihydrogen peroxide; potassium carbonate; In 1-methyl-pyrrolidin-2-one; acetic acid;
DOI:10.1023/A:1022563529344