4-Phenylisothiazolidine 1,1-dioxide

Base Information

Chemical Name:4-Phenylisothiazolidine 1,1-dioxide
CAS No.:320393-23-5
Molecular Formula:C₉H₁₁NO₂S
Molecular Weight:197.258
Hs Code.:
European Community (EC) Number:869-819-6

Synonyms:4-Phenylisothiazolidine 1,1-dioxide;320393-23-5;4-phenyl-1,2-thiazolidine 1,1-dioxide;4-phenyl-1,2-thiazolidine-1,1-dione;SCHEMBL2979492;CAGITIWEIXFGFH-UHFFFAOYSA-N;4-Phenylisothiazolidine1,1-dioxide;4-phenyl-isothiazolidine 1,1-dioxide;AKOS027196482;CS-0132631;4-phenyl-1lambda6,2-thiazolidine-1,1-dione;EN300-211206;Z1862025182

Suppliers and Price of 4-Phenylisothiazolidine 1,1-dioxide

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 3 raw suppliers

Chemical Property of 4-Phenylisothiazolidine 1,1-dioxide

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:197.05104977
Heavy Atom Count:13
Complexity:262

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(CS(=O)(=O)N1)C2=CC=CC=C2

Technology Process of 4-Phenylisothiazolidine 1,1-dioxide

There total 4 articles about 4-Phenylisothiazolidine 1,1-dioxide 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: 63.0%

: 320393-21-3
3-amino-2-phenylpropane-1-sulfonic acid phenyl ester

: 320393-23-5
4-phenylsultam

Guidance literature:: With potassium hydroxide; In 1,4-dioxane; water; at 18 ℃; for 24h;
DOI:10.1007/BF02508284

Reference yield:

: 13719-31-8
phenyl β-styrenesulfonate

: 320393-23-5
4-phenylsultam

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium methylate / dimethylsulfoxide

1.2: 70 percent / dimethylsulfoxide / 24 h / 20 °C

2.1: 62 percent / H₂ / Raney nickel / 24 h / 20 °C / 760 Torr

3.1: 63 percent / KOH / dioxane; H₂O / 24 h / 18 °C

With potassium hydroxide; hydrogen; sodium methylate; nickel; In 1,4-dioxane; water; dimethyl sulfoxide;
DOI:10.1007/BF02508284

Reference yield:

: 4091-26-3
β-styrenesulfonyl chloride

: 320393-23-5
4-phenylsultam

Guidance literature:: Multi-step reaction with 4 steps

1.1: Na

2.1: sodium methylate / dimethylsulfoxide

2.2: 70 percent / dimethylsulfoxide / 24 h / 20 °C

3.1: 62 percent / H₂ / Raney nickel / 24 h / 20 °C / 760 Torr

4.1: 63 percent / KOH / dioxane; H₂O / 24 h / 18 °C

With potassium hydroxide; hydrogen; sodium methylate; sodium; nickel; In 1,4-dioxane; water; dimethyl sulfoxide;
DOI:10.1007/BF02508284