3-(Benzenesulfonyl)cyclohex-2-en-1-one

Base Information

Chemical Name:3-(Benzenesulfonyl)cyclohex-2-en-1-one
CAS No.:88036-12-8
Molecular Formula:C12H12O3S
Molecular Weight:236.291
Hs Code.:
DSSTox Substance ID:DTXSID70502309
Wikidata:Q82355222

Synonyms:3-(Benzenesulfonyl)cyclohex-2-en-1-one;88036-12-8;DTXSID70502309

Suppliers and Price of 3-(Benzenesulfonyl)cyclohex-2-en-1-one

Supply Marketing:

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

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Chemical Property of 3-(Benzenesulfonyl)cyclohex-2-en-1-one

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:236.05071541
Heavy Atom Count:16
Complexity:395

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 3-(Benzenesulfonyl)cyclohex-2-en-1-one

There total 7 articles about 3-(Benzenesulfonyl)cyclohex-2-en-1-one 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: 91.0%

: 75717-39-4
3-(phenylsulfanyl)cyclohex-2-en-1-one

: 88036-12-8
3-(Phenylsulfonyl)-2-cyclohexen-1-one

Guidance literature:: With Oxone; In methanol; water; for 4h; Ambient temperature;
DOI:10.1021/ja00201a032

Reference yield: 71.0%

: 94404-09-8
(4-Benzenesulfonyl-5-methylene-cyclohex-1-enyloxy)-trimethyl-silane

: 88036-12-8
3-(Phenylsulfonyl)-2-cyclohexen-1-one

Guidance literature:: at 180 ℃; for 2h; under 1 Torr;
DOI:10.1021/jo00204a018

Reference yield:

: 504-02-9
1,3-cylohexanedione

: 88036-12-8
3-(Phenylsulfonyl)-2-cyclohexen-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / TsOH / benzene

2: 91 percent / oxone / methanol; H₂O / 4 h / Ambient temperature

With Oxone; toluene-4-sulfonic acid; In methanol; water; benzene;
DOI:10.1021/ja00201a032