Application of 67686-01-5, 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.67686-01-5, Name is (1-Benzylpiperidin-4-yl)methanol, molecular formula is C13H19NO. In a article，once mentioned of 67686-01-5
5, 6 – dimethoxy – 1 – oxo – 2, 3 – dihydro – 1H – indene – 2 – to (a) the present invention refers to a group represented by the formula 3 formula 4 […][…] represented benzylpiperidine compound reacting to the presence of a base, to 2 – oxo – 5, 6 – dimethoxy – 1 – ((1 – benzylpiperidine – 4 – yl) methyl) represented by the formula 2 – 2, 3 – dihydro – 1H – indene – 2 – […][…] step number tank; and (b) 2 – oxo – 5, 6 – dimethoxy – 1 – ((1 – benzylpiperidine – 4 – yl) methyl) of said formula 2 formula 1 – 2, 3 – dihydro – 1H – indene – 2 – de […][…] hydrocyanation reaction (decyanation reaction) of a method including the step number it goes roundlung questionlung qualityit goes round caused by representative number bath tank number under public affairs substrate. (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 67686-01-5, and how the biochemistry of the body works.Application of 67686-01-5
Reference：
Piperidine – Wikipedia,
Piperidine | C5H15266N – PubChem