Comparison of Chirasil-DEX CB as gas chromatographic and ULMO as liquid chromatographic chiral stationary phase for enantioseparation of aryl- and heteroarylcarbinols was written by Uray, G.;Stampfer, W.;Fabian, W. M. F.. And the article was included in Journal of Chromatography, A in 2003.COA of Formula: C8H9ClO This article mentions the following:
For a broad spectrum of simple chiral alcs., incorporating a (substituted) (het)aryl building block, enantiomer separation characteristics are reported for both gas chromatog. on a Chirasil-DEX phase, and liquid chromatog. on an (S,S)-ULMO phase. On this chiral Pirkle-type phase, homochiral enantiomers (mostly R) are eluted 1st without exception. The elution order R before S appears conserved as a rule also for gas chromatog. separations on Chirasil-DEX, though with some remarkable exceptions indicating a change in the dominant discriminative mechanism. This was shown in the homologous series 1-phenylethanol to 1-phenylhexanol having the point of reversal at C4, while the o-methoxy analogs elute from C1 to C4 already in the reversed order. In the experiment, the researchers used many compounds, for example, (R)-1-(3-Chlorophenyl)ethanol (cas: 120121-01-9COA of Formula: C8H9ClO).
(R)-1-(3-Chlorophenyl)ethanol (cas: 120121-01-9) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.COA of Formula: C8H9ClO
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts