Reference of 2359-60-6, 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.2359-60-6, Name is 4-Piperidinoaniline, molecular formula is C11H16N2. In a article，once mentioned of 2359-60-6
4-Dimethylamino-, 4-pyrrolidino-, 4-piperidino-, 4-morpholino- and 4-(4-methylpiperazino)thiophenol (IIIa-IIIe), which were prepared by two methods and characterized as the 2,4-dinitrodiphenyl sulfides IVb-IVe, were transformed by treatment with 2-iodobenzoic acid and copper in aqueous potassium hydroxide to 2-(4-tert.aminophenylthio)benzoic acids (Va-Ve).Cyclization with polyphosphoric acid gave thioxanthones VIa-VIe which were treated with 3-dimethylaminopropylmagnesium chloride to give the diamino alcohols VIIa-VIId.VIIa, VIIc and VIId were dehydrated by heating with dilute sulfuric acid which resulted in mixtures of geometrical isomers of the olefinic bases Ia, Ic and Id.Crystallization of bases or salts led to homogeneous or almost homogeneous (Z)-isomers belonging to the “active chlorprothixene series”.The products are devoid of cataleptic and antiapomorphine activities and show only some properties of mild tranquillizers.
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Reference：
Piperidine – Wikipedia,
Piperidine | C5H10646N – PubChem