1-Chloro-2-(ethenesulfonyl)benzene

Base Information

Chemical Name:1-Chloro-2-(ethenesulfonyl)benzene
CAS No.:5535-44-4
Molecular Formula:C8H7ClO2S
Molecular Weight:202.661
Hs Code.:
NSC Number:202737
DSSTox Substance ID:DTXSID50308225
Wikidata:Q82055988

Synonyms:5535-44-4;1-Chloro-2-(ethenesulfonyl)benzene;NSC202737;SCHEMBL3387970;DTXSID50308225;AKOS012250039;NSC-202737

Suppliers and Price of 1-Chloro-2-(ethenesulfonyl)benzene

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 4 raw suppliers

Chemical Property of 1-Chloro-2-(ethenesulfonyl)benzene

Chemical Property:

Vapor Pressure:8.65E-05mmHg at 25°C
Boiling Point:350.9°Cat760mmHg
Flash Point:166°C
Density:1.309g/cm³
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:201.9855283
Heavy Atom Count:12
Complexity:253

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CS(=O)(=O)C1=CC=CC=C1Cl

Technology Process of 1-Chloro-2-(ethenesulfonyl)benzene

There total 5 articles about 1-Chloro-2-(ethenesulfonyl)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:

: 1822-73-7
phenylthioethylene

: 5535-44-4
1-Chloro-2-ethenesulfonyl-benzene

: 20451-53-0,88180-53-4,89299-86-5,89299-85-4
(-)-(S)_S-phenyl vinyl sulfoxide

: 89299-86-5
(+)-(R)_S-phenyl vinyl sulfoxide

Guidance literature:: phenylthioethylene; In aq. phosphate buffer; at 20 ℃; for 5h; pH=5.1;

With dihydrogen peroxide; In water; at 0 ℃; for 28h;
DOI:10.1039/c5dt04507j

Reference yield:

: 6320-03-2
2-chlorothiphenol

: 5535-44-4
1-Chloro-2-ethenesulfonyl-benzene

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / acetonitrile / 20 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C

3: triethylamine / dichloromethane / 0.5 h

With caesium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; acetonitrile;
DOI:10.1039/d1gc03482k

Reference yield:

: 3983-75-3
(2-bromoethyl)(2-chlorophenyl)sulfane

: 5535-44-4
1-Chloro-2-ethenesulfonyl-benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C

2: triethylamine / dichloromethane / 0.5 h

With triethylamine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1039/d1gc03482k