Reference of 6789-94-2, 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.6789-94-2, Name is 1-Ethylpiperidin-3-amine, molecular formula is C7H16N2. In a article，once mentioned of 6789-94-2
Novel quinazoline and cinnoline derivatives having the formula STR1 (wherein one of A and B is CH and the other one of A and B is N; X1 is halogen or CF3 and X3 is one of the groups II, III, IV or V STR2 where Q is lower alkylene; R1 is hydrogen or lower alkyl; R2 and R3 are independently lower alkyl or R2 and R3 are a divalent radical such that HNR2 R3 is a secondary cyclic amine with 5 to 7 ring atoms; R4 is lower alkyl; n is 0 or 1; the rings shown in formulae III and IV are piperidine or pyrrolidine optionally substituted by lower alkyl; and the ring shown in formula V is piperazine optionally substituted by lower alkyl) and their pharmaceutically acceptable salts are useful as pharmaceuticals particularly as anti-hypertensives. Novel intermediates are also described including the corresponding sulphonic acids of formula I (where A, B and X1 are defined above and X3 is OH).
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 6789-94-2, and how the biochemistry of the body works.Reference of 6789-94-2
Reference：
Piperidine – Wikipedia,
Piperidine | C5H4030N – PubChem