Simple exploration of Methyl 2-piperidinecarboxylate

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.Reference of 41994-45-0, you can also check out more blogs about41994-45-0

Reference of 41994-45-0, 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. 41994-45-0, Name is Methyl 2-piperidinecarboxylate, molecular formula is C7H13NO2. In a Article,once mentioned of 41994-45-0

When N-methoxycarbonyl and N-benzoxycarbonyl derivatives of methyl esters of aziridine-2-carboxylic acid, L-proline, L-thioproline, and pipecolic acid interact with NaBH4 in tert-butanol/methanol, the products of reduction of the C-methoxycarbonyl group of the original compounds are accompanied by bicyclic urethanes and oxazolidines.Reduction of N-maleates and N-fumarates of heterocyclic alpha-iminocarboxylic acids leads to the formation of alpha-hydroxymethyl-N-<4-(2-oxo-2,5-dihydrofuryl)> derivatives of pyrrolidine, piperidine, 1,3-thiazolidine, and 1,4-thiazan.In the latter case, 1-aza-2 -hydroxymethyl-4-oxo-5-oxa-9-thiabicyclo<5.4.0>undecene-2 is also obtained.The N-maleates and fumarates of aziridine-2-carboxylic acid are reduced anomalously by sodium borohydride, forming 2-hydroxymethyl-2-(beta-hydroxyethyl)-3-oxa-1-azabicyclo<3.1.0>hexanes

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.Reference of 41994-45-0, you can also check out more blogs about41994-45-0

Reference:
Piperidine – Wikipedia,
Piperidine | C5H7061N – PubChem