Electric Literature of 5799-75-7, 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.5799-75-7, Name is 1-(Prop-2-yn-1-yl)piperidine, molecular formula is C8H13N. In a article，once mentioned of 5799-75-7
A novel 1,3-amino group migration strategy for the synthesis of acrylamidines is presented. Cu(i) catalyzed reaction of N,N-disubstituted propargylamine with tosylazide generates a highly reactive ketenimine intermediate which is trapped by a tethered amino group leading to the rearrangement reaction.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 5799-75-7, and how the biochemistry of the body works.Electric Literature of 5799-75-7
Reference：
Piperidine – Wikipedia,
Piperidine | C5H3211N – PubChem