Some scientific research about 147636-36-0

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.Application of 147636-36-0, you can also check out more blogs about147636-36-0

Application of 147636-36-0, 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. 147636-36-0, Name is 1-Tosylpiperidine-4-carboxylic acid, molecular formula is C13H17NO4S. In a Article,once mentioned of 147636-36-0

An one-pot reaction of carboxylic acids and ynol ethers for the synthesis of beta-keto esters has been developed. Under promotion of Ag2O, various carboxylic acids and ynol ethers could transform to alpha-acyloxy enol esters, which undergo a following DMAP-catalyzed rearrangement to deliver beta-keto esters rapidly. This method provides a direct approach to beta-keto esters from carboxylic acids without any preactivation. The protocol features mild reaction conditions, broad substrate scope, and the products could be transformed to an array of compounds.

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.Application of 147636-36-0, you can also check out more blogs about147636-36-0

Reference:
Piperidine – Wikipedia,
Piperidine | C5H22701N – PubChem