Ethyl 2,2-dimethylpropane-1-sulfonate

Base Information

Chemical Name:Ethyl 2,2-dimethylpropane-1-sulfonate
CAS No.:13304-66-0
Molecular Formula:C7H16O3S
Molecular Weight:180.2651
Hs Code.:
NSC Number:23364
DSSTox Substance ID:DTXSID80281890
Wikidata:Q82016004

Synonyms:13304-66-0;ethyl 2,2-dimethylpropane-1-sulfonate;NSC23364;DTXSID80281890;NSC 23364;NSC-23364

Suppliers and Price of Ethyl 2,2-dimethylpropane-1-sulfonate

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 Ethyl 2,2-dimethylpropane-1-sulfonate

Chemical Property:

Vapor Pressure:0.0165mmHg at 25°C
Boiling Point:263.7°Cat760mmHg
Flash Point:113.3°C
Density:1.05g/cm³
XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:180.08201554
Heavy Atom Count:11
Complexity:193

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOS(=O)(=O)CC(C)(C)C

Technology Process of Ethyl 2,2-dimethylpropane-1-sulfonate

There total 6 articles about Ethyl 2,2-dimethylpropane-1-sulfonate 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:

: 463-82-1
2,2-dimethylpropane

: 13304-66-0
2,2-dimethyl-propane-1-sulfonic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: tetrachloromethane; sulfur dioxide; chlorine / unter Belichtung

3: diethyl ether

With tetrachloromethane; diethyl ether; sulfur dioxide; chlorine;
DOI:10.1021/jo01110a002