Miklas, R. published the artcileSynthesis and antimicrobial properties of camphorsulfonic acid derived imidazolium salts, Synthetic Route of 21286-54-4, the publication is Acta Facultatis Pharmaceuticae Universitatis Comenianae (2014), 61(2), 42-48, database is CAplus.
A group of homochiral imidazolium salts bearing hydrophobic camphorsulfonyl alkyl esters I [R = decyl, dodecyl, tetradecyl] or amides II were synthesized and characterized. The novel imidazolium bromides were tested as antimicrobial and antifungal agents and their minimal inhibitory concentration (MIC) was evaluated and compared to clin. used benzalkonium bromide (BAB) and carbethopendecinium bromide. The MIC values of amide derivatives II [R = decyl, dodecyl] were slightly smaller than those for BAB, indicating their good activity. None of the prepared salts was more effective than carbethopendecinium bromide. The biocidal efficacy of amide derivatives was much higher when compared to the ester analogs.
Acta Facultatis Pharmaceuticae Universitatis Comenianae published new progress about 21286-54-4. 21286-54-4 belongs to chlorides-buliding-blocks, auxiliary class Chiral,Chloride,Sulfonyl chlorides,Aliphatic cyclic hydrocarbon,Ketone, name is ((1S,4R)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonyl chloride, and the molecular formula is C10H15ClO3S, Synthetic Route of 21286-54-4.
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