Trimethylsulfonium

Base Information

Chemical Name:Trimethylsulfonium
CAS No.:676-84-6
Molecular Formula:C3H9NO3S
Molecular Weight:77.1705
Hs Code.:
UNII:8U5M0SJV65
DSSTox Substance ID:DTXSID50862857
Nikkaji Number:J257.549C
Wikipedia:Trimethylsulfonium
Wikidata:Q7842221
Metabolomics Workbench ID:41978
ChEMBL ID:CHEMBL1237171
Mol file:676-84-6.mol

Synonyms:trimethylsulfonium;trimethylsulfonium chloride;trimethylsulfonium hydroxide;trimethylsulfonium iodide;trimethylsulfonium nitrate;trimethylsulphonium chloride

Suppliers and Price of Trimethylsulfonium

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 5 raw suppliers

Chemical Property of Trimethylsulfonium

Chemical Property:

PSA：25.30000
LogP:-2.50190
Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere
Solubility.:Methanol (Slightly), Water (Slightly)
XLogP3:0.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:77.04249646
Heavy Atom Count:4
Complexity:8

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[S+](C)C
Uses Trimethylsulfonium Chloride is used as a reagent in the preparation of spirastrellolide A Me ester via Suzuki coupling, Yamaguchi lactonization, Julia-Kocienski olefination, bond cleavage, and ozonolysis, its antitumor activity, and SAR with truncated variants.

Technology Process of Trimethylsulfonium

There total 2 articles about Trimethylsulfonium 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: 44.0%

: 887144-94-7
Togni's reagent II

: 67-68-5,8070-53-9
dimethyl sulfoxide

: 98-83-9,6144-04-3,25014-31-7,42612-14-6
isopropenylbenzene

: 676-84-6
trimethylsulfonium

: 709-21-7
3,3,3-trifluoro-1-phenylpropan-1-one

Guidance literature:: With tris[2-phenylpyridinato-C₂,N]iridium(III); at 20 ℃; for 2h; Irradiation; Green chemistry;
DOI:10.1016/j.crci.2015.01.013