Extracurricular laboratory: Synthetic route of 60827-45-4

When you point to this article, it is believed that you are also very interested in this compound(60827-45-4)Synthetic Route of C3H7ClO2 and due to space limitations, I can only present the most important information.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 60827-45-4, is researched, SMILESS is OC[C@H](O)CCl, Molecular C3H7ClO2Journal, Czech Journal of Food Sciences called Optical isomers of chloropropanediols: mechanisms of their formation and decomposition in protein hydrolyzates, Author is Velisek, Jan; Dolezal, Marek; Crews, Colin; Dvorak, Tomas, the main research direction is chloropropanediol enantiomer formation.Synthetic Route of C3H7ClO2.

Protein hydrolyzates produced by HCl 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 experiments with glycerol, triolein and soy lecithin heated with HCl in solution showed that these materials were precursors of 3-chloropropane-1,2-diol and 2-chloropropane-1,3-diol and, as expected, yielded racemic 3-chloropropane-1,2-diol. Yields of 3-chloropropane-1,2-diols decreased in the order triolein > lecithin > glycerol. The mechanisms of 3-chloropropane-1,2-diol enantiomers formation during the production of protein hydrolyzates are presented and discussed as well as the reaction pathways of their decomposition in alk. media via the corresponding intermediates, (R)- and (S)-glycidol, resp. Both epoxides are hydrolyzed to glycerol and form a variety of products with hydrolyzate constituents.

When you point to this article, it is believed that you are also very interested in this compound(60827-45-4)Synthetic Route of C3H7ClO2 and due to space limitations, I can only present the most important information.

Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com