Xia, Li-Jun; Tang, Min-Hua; Hu, Jian-Bing; Ding, Zuo-Ding; Jin, Hao; Zhao, Gang published an article on January 31 ,2002. The article was titled ãEnantiomeric resolution of secondary aromatic alcohols and arylethanediols by HPLC on chiral stationary phaseã? and you may find the article in Youji Huaxue.SDS of cas: 133082-13-0 The information in the text is summarized as follows:
Separation of racemic mixtures of thirty-eight secondary aromatic alcs. and arylethanediols with different substituting group was achieved with HPLC by using Chiralcel OD and Chiralcel OJ as chiral stationary phase and hexane/2-propanol mixtures of different ratios as eluents. The chromatog. parameters of these racemates on OD and OJ columns were examined The results showed enantiomeric resolution ability of the racemic mixtures on these columns was strongly dependent on the site and the property of substituents. The hydrogen bonding and π-π interactions between the chiral stationary phase and the polar group of secondary aromatic alcs. and arylethanediols may be responsible for the chiral resolution This method had been applied to determination of the optical purity of the asym. reduction products of prochiral ketones. In the experiment, the researchers used many compounds, for example, (1S)-1-(2-chlorophenyl)ethane-1,2-diol(cas: 133082-13-0SDS of cas: 133082-13-0)
(1S)-1-(2-chlorophenyl)ethane-1,2-diol(cas: 133082-13-0) belongs to hydroxy-containing compounds. Hydroxy groups participate in the dehydration reactions that link simple biological molecules into long chains.SDS of cas: 133082-13-0 The joining of a fatty acid to glycerol to form a triacylglycerol removes the −OH from the carboxy end of the fatty acid.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts