In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Three different types of chirality-driven crystallization within the series of uniformly substituted phenyl glycerol ethers, published in 2008-11-30, which mentions a compound: 60827-45-4, mainly applied to chirality driven crystallization uniformly phenyl glycerol ether crystallog, HPLC of Formula: 60827-45-4.
Seven chiral aryl glycerol ethers 2-R-C6H4-O-CH2CH(OH)CH2OH (R = H, Me, Et, Allyl, n-Pr, i-Pr, tert-Bu) were synthesized in racemic and scalemic form. The IR spectra, m.ps., and enthalpies of fusion for racemic and scalemic samples of every species were measured, the entropies of enantiomers mixing in the liquid state and Gibbs free energies of a racemic compound formation were derived and binary phase diagrams were reconstructed for the whole family. Solid racemic compounds stabilities were ranked for the four substances. Spontaneous resolution was established for the registered chiral drug mephenesin and its Et analog. Metastable anomalous conglomerate, forming crystals having three independent R* and one independent S* mols. in the unit cell, is formed during solution crystallization of tert-Bu derivative; metastable phase transforms slowly into traditional racemic conglomerate.
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Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com