Application of 1000796-62-2, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1000796-62-2, Name is tert-Butyl 3-aminopiperidine-1-carboxylate hydrochloride, molecular formula is C10H21ClN2O2. In a article，once mentioned of 1000796-62-2
The kinetic resolution of 3-aminopyrrolidine (3AP) and 3-aminopiperidine (3APi) with omega-transaminases was facilitated by the application of a protecting group concept. 1-N-Cbz-protected 3-aminopyrrolidine could be resolved with >99% ee at 50% conversion, the resolution of 1-N-Boc-3-aminopiperidine yielded 96% ee at 55% conversion. The reaction rate was up to 50-fold higher by using protected substrates. Most importantly, enantioselectivity increased remarkably after carbamate protection compared to the unprotected substrates (86 vs. 99% ee). Surprisingly, benzyl protection of 3AP had no influence on enantioselectivity. A possible explanation for this observation could be the different flexibility of the benzyl- or carbamate-protected 3AP as confirmed by NMR spectroscopy.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 1000796-62-2, and how the biochemistry of the body works.Application of 1000796-62-2
Reference：
Piperidine – Wikipedia,
Piperidine | C5H19166N – PubChem