Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 60827-45-4, is researched, Molecular C3H7ClO2, about Optical isomers of chloropropanols: Mechanisms of their formation and decomposition in foods, the main research direction is protein hydrolyzate chloropropanol enantiomer.Recommanded Product: (2S)-(+)-3-Chloropropane-1,2-diol.
Protein hydrolyzates produced by hydrochloric acid hydrolysis were analyzed for 3-chloropropane-1,2-diol and its enantiomers. It was found that (R)-3-chloropropane-1,2-diol and (S)-3-chloropropane-1,2-diol were present in the hydrolyzates in equimolar concentrations Model system experiments with glycerol, triolein and soy lecithin heated with hydrochloric acid in solution showed that these materials were precursors of 3-chloropropane-1,2-diol and yielded racemic mixtures of its enantiomers. Yields of 3-chloropropane-1,2-diols decreased in the order triolein > lecithin > glycerol. Mechanisms of 3-chloropropane-1,2-diol enantiomer formation during the production of protein hydrolyzates are presented and discussed as well as reaction pathways of their decomposition in alk. media via the corresponding (R)- and (S)-hydroxymethyloxiranes. In alk. media both 3-chloropropane-1,2-diol enantiomers decomposed at the same rate.
In addition to the literature in the link below, there is a lot of literature about this compound((2S)-(+)-3-Chloropropane-1,2-diol)Recommanded Product: (2S)-(+)-3-Chloropropane-1,2-diol, illustrating the importance and wide applicability of this compound(60827-45-4).
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com