Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 53562-86-0, is researched, Molecular C5H10O3, about Studies of co-modifier and carboxylic acid for the enantio-differentiating hydrogenation of 2-octanone over a tartaric acid in situ modified nickel catalyst, the main research direction is hydrogenation octanone tartarate nickel catalyst sodium pivalate.Product Details of 53562-86-0.
The effects of a co-modifier and carboxylic acid on the hydrogenation rate and the enantio-differentiating ability (e.d.a.) were studied for the hydrogenation of 2-octanone and Me acetoacetate over a tartaric acid modified reduced nickel catalyst. For the hydrogenation of 2-octanone, tartaric acid, pivalic acid, and Na+ were necessary for the appearance of the predominant e.d.a. Sodium pivalate, instead of the typical co-modifier, NaBr, was appropriate for the in situ modification of reduced nickel. The use of sodium pivalate resulted in a higher hydrogenation rate and e.d.a.
After consulting a lot of data, we found that this compound(53562-86-0)Product Details of 53562-86-0 can be used in many types of reactions. And in most cases, this compound has more advantages.
Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics