Recommanded Product: 60827-45-4. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (2S)-(+)-3-Chloropropane-1,2-diol, is researched, Molecular C3H7ClO2, CAS is 60827-45-4, about Simultaneous production of chirally enriched epoxides and 1,2-diols from racemic epoxides via hydrolytic kinetic resolution. Author is Kureshy, R. I.; Khan, N. H.; Abdi, S. H. R.; Patel, S. T.; Jasra, R. V..
Hydrolytic kinetic resolution of racemic epichlorohydrin, styrene oxide and propene oxide was investigated using a dimeric homochiral Co(III) Schiff base complex derived from the monotartrate salt of (1R,2R)-(-)-cyclohexanediamine with 3,5-di-tert-butylsalicylaldehyde and 5,5′-methylenebis[3-tert-butylsalicylaldehyde] to get high efficiency and recycling capability of the catalyst. Excellent conversions to enantiomerically pure epoxide and diols along with high chiral induction were obtained in all cases. With a loading of <0.3 mol % of the catalyst, the system works well for up to three cycles without any loss in activity and selectivity. Compounds in my other articles are similar to this one((2S)-(+)-3-Chloropropane-1,2-diol)Recommanded Product: 60827-45-4, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com