Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Chemistry & Industry (London, United Kingdom) called Stereospecific synthesis of R- and S-3-chloropropan-1,2-diol, Author is Jones, Haydn F., which mentions a compound: 60827-45-4, SMILESS is OC[C@H](O)CCl, Molecular C3H7ClO2, Recommanded Product: (2S)-(+)-3-Chloropropane-1,2-diol.
S-ClCH2CH(OH)CH2OH (S-I) was prepared from Me 6-chloro-6-deoxy-α-D-glucopyranoside by sequential oxidative ring cleavage, reduction and hydrolysis. R-I was similarly prepared from Me 5-chloro-5-deoxy-α-L-arabinofuranoside, which was obtained from Me 2,3-di-O-benzoyl-5-O-(p-tolylsulfonyl)-α-L-arabinofuranoside by chlorination and then deesterification.
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Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com