Benzene, (1-cyclobuten-1-ylsulfonyl)-

Base Information

Chemical Name:Benzene, (1-cyclobuten-1-ylsulfonyl)-
CAS No.:163706-67-0
Molecular Formula:C10H10O2S
Molecular Weight:194.254
Hs Code.:
DSSTox Substance ID:DTXSID10447644
Nikkaji Number:J814.778G
Wikidata:Q82266518
Mol file:163706-67-0.mol

Synonyms:Benzene, (1-cyclobuten-1-ylsulfonyl)-;163706-67-0;(1-cyclobuten-1-ylsulfonyl)benzene;1-cyclobutenylsulfonyl-benzene;1-Cyclobuten-1-ylphenyl sulfone;(Cyclobut-1-enesulfonyl)-benzene;DTXSID10447644

Suppliers and Price of Benzene, (1-cyclobuten-1-ylsulfonyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Benzene, (1-cyclobuten-1-ylsulfonyl)-

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:194.04015073
Heavy Atom Count:13
Complexity:302

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(=C1)S(=O)(=O)C2=CC=CC=C2

Technology Process of Benzene, (1-cyclobuten-1-ylsulfonyl)-

There total 6 articles about Benzene, (1-cyclobuten-1-ylsulfonyl)- 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: 82.7%

: 5535-48-8
PVS

: 163706-67-0
(Cyclobut-1-enesulfonyl)-benzene

Guidance literature:: With N,N,N,N-tetraethylammonium tetrafluoroborate; In acetonitrile; Electrolysis;
DOI:10.1016/j.tetlet.2007.11.171

Reference yield: 70.0%

: 128176-20-5
trans-1,2-bis(phenylsulfonyl)cyclobutane

: 163706-67-0
(Cyclobut-1-enesulfonyl)-benzene

Guidance literature:: With oxygen; tetraethylammonium perchlorate; In N,N-dimethyl-formamide; Ambient temperature; electrogenerated (Hg cathodically) elimination;
DOI:10.1016/0040-4039(95)00225-2