Archives for Chemistry Experiments of 1-Aminopiperidine

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.Synthetic Route of 2213-43-6, you can also check out more blogs about2213-43-6

Synthetic Route of 2213-43-6, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 2213-43-6, Name is 1-Aminopiperidine, molecular formula is C5H12N2. In a Article，once mentioned of 2213-43-6

Aldehyde and ketone N,N-dialkylhydrazones behave as a stable class of imine surrogates exhibiting a unique reactivity in the Strecker reaction with in situ generated HCN, that proceeds in pure water in the absence of co-solvents, catalysts or promoters. Experimental evidence suggests that the reaction is assisted by an intramolecular activation of HCN by the dialkyl amino lone pair. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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.Synthetic Route of 2213-43-6, you can also check out more blogs about2213-43-6

Reference：
Piperidine – Wikipedia,
Piperidine | C5H1044N – PubChem