A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Safety of tert-Butyl 4-(hydroxyimino)piperidine-1-carboxylate, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 150008-24-5, Name is tert-Butyl 4-(hydroxyimino)piperidine-1-carboxylate, molecular formula is C10H18N2O3. In a Article, authors is Mullen, Philip，once mentioned of 150008-24-5
Previously unreported N-Boc 4-nitropiperidine was prepared in two steps from N-Boc-piperidone. The synthetic utility of this new intermediate was demonstrated by the development of a new and simple route to spirolactam piperidines. Further synthetic work involving a challenging triazole cyclisation allowed the preparation of a spiropiperidine analogue of the eastern part of maraviroc.
Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about is helpful to your research. Safety of tert-Butyl 4-(hydroxyimino)piperidine-1-carboxylate
Reference：
Piperidine – Wikipedia,
Piperidine | C5H16664N – PubChem