Reference of 26371-07-3, 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.26371-07-3, Name is 3-(Piperidin-1-yl)propanoic acid, molecular formula is C8H15NO2. In a article，once mentioned of 26371-07-3
After solvent evaporation 1 – (3 – (3 – (4 – of) chlorophenyl) propyl) piperidine – 1 1-yl, propionic acid solution :S1, is added into the reactor 3 – (4 – to react)-chlorophenyl-3 – (-propyl-)-propan ;S2,yl, propionic acid solution 3 – (4 – to)-chlorophenyl-3 – (-propynyl) piperi- 1 1-yl, propionate solution . The method comprises the following steps 3 – (4 – preparing)-chlorophenoxy-3 – (-propan) piperi- 1 1-yl) ;S3, propionate in a reactor at a certain temperature 3 – (4 – and) adding a solid super strong acid) to obtain ;S4, the target product 3 – (-), phenyl)-propoxy-propyl 3 – (4 -) piperidinetanyl hydrochloride. 3 – (4 -)). 3 – (The. invention is low in cost 1 – (3 – (3 – (4 – 3 – (yield))-yl propionate 50-70 C, toluene 4-8 solution by adding a solid super-strong acid. (by machine translation)
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 26371-07-3, and how the biochemistry of the body works.Reference of 26371-07-3
Reference：
Piperidine – Wikipedia,
Piperidine | C5H9182N – PubChem