Reference of 1484-84-0, 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.1484-84-0, Name is 2-Piperidineethanol, molecular formula is C7H15NO. In a article，once mentioned of 1484-84-0
Treatment of 2-(2′-alkenyl)-piperidine boranes with iodine or triflic acid induces internal hydroboration with high regiocontrol, even with a terminal alkene (R H). Good stereocontrol is possible for the N-benzyl substrates. Comparisons with acyclic model structures show that the source of regiocontrol with the terminal alkene is due to a steric effect of the axial piperidine C(3,5) hydrogens that destabilize the competing bridged bicyclic transition state.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 1484-84-0, and how the biochemistry of the body works.Reference of 1484-84-0
Reference：
Piperidine – Wikipedia,
Piperidine | C5H5485N – PubChem