Chemistry is traditionally divided into organic and inorganic chemistry. Product Details of 18531-99-2. The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent，Which mentioned a new discovery about 18531-99-2
The determination of the enantiomeric composition of chiral compounds by 1H, 13C, and 31P NMR spectroscopy in the presence of (S)-1,1′-binaphthyl-2,2′-diol demonstrated that the enantioselectivity of the method increases when the polarity of a solvent decreases as follows: CD3OD-D2O (4:1) < CD3OD < CDCl3 < CDCl3-CCl4 (1:1) < C6D6.The effect is caused by increase in stability of solvating agent-substrate complexes formed through the hydrogen bonds.Pantolactone, esters of substituted cyclopropanecarboxylic acids, amino alcohol propranolol, and 2,2'-bis(diphenylphosphinyl)-1,1'-binaphthyl were used as the substrates. Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 18531-99-2, you can also check out more blogs about18531-99-2
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI