20686-91-3Relevant articles and documents
A comparative study of the electrochemical fluorination (ECF) of 1 ,n-alkanebis (sulfonylfluorides) (n = 1-3 )
Jueschke, Ralf,Velayutham, David,Sartoria, Peter
, p. 145 - 149 (1997)
Synthetic methods for the preparation of α,ω-alkanebis(sulfonylfluorides) and their electrochemical fluorination (ECF) are described in detail. Factors affecting the yield of the perfluoro-α,ω-alkanebis(sulfonylfluorides) are also discussed. Spectral data (13C and 19F NMR and mass spectra) and other hitherto unknown physical properties of difluoromethanebis(sulfonylfluoride) (1), 1,1,2,2-tetrafluoroethane-1,2-bis(sulfonylfluoride) (2) and 1,1,2,2,3,3-hexafluoropropane-1,3-bis(sulfonylfluoride) (3) are measured and compared. Elsevier Science S.A.
Clean and economic synthesis of alkanesulfonyl chlorides from S-alkyl isothiourea salts via bleach oxidative chlorosulfonation
Yang, Zhanhui,Zhou, Bingnan,Xu, Jiaxi
, p. 225 - 229 (2014/03/21)
A simple procedure for clean and economic synthesis of alkanesulfonyl chlorides via bleach-mediated oxidative chlorosulfonation of S-alkyl isothiourea salts is disclosed. This procedure is environment- and worker-friendly with the advantages of readily accessible materials and reagents, simple and safe operations, easy purification without chromatography, and affords high yields of up to 99%.
METHODS, COMPOUNDS, AND COMPOSITIONS FOR DELIVERING 1,3-PROPAN ED ISULFONIC ACID
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Page/Page column 64, (2011/02/24)
The invention relates to methods, compounds, and compositions for delivering 1,3-propanedisulfonic acid (1,3PDS) in a subject, preferably a human subject. The invention encompasses compounds that will yield or generate 1,3PDS, either in vitro or in vivo. The invention also relates to sulfonate ester prodrugs of 1,3PDS as well as Gemini dimmers and oligomers of 1,3PDS for the prevention or treatment of associated diseases and conditions.