Simple exploration of 2-(Piperidin-4-yl)-1H-benzo[d]imidazole

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Related Products of 38385-95-4, you can also check out more blogs about38385-95-4

Related Products of 38385-95-4, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 38385-95-4, Name is 2-(Piperidin-4-yl)-1H-benzo[d]imidazole, molecular formula is C12H15N3. In a Patent,once mentioned of 38385-95-4

The present invention discloses a process for the preparation of drugs for treating liver cancer of the aryl residue ruthenium complex, the aryl residue ruthenium complexes of the chemical name is: (2 – (4 – (N – (5 – diethylene glycol double (2 – propynyl) ether) indazolyl piperidinyl)) benzimidazolyl) methyl isopropyl the benzene gathers the ruthenium (II), the structural formula is: The invention also discloses the preparation of aryl residue ruthenium complex method and a plurality of application. Aryl residue ruthenium complexes of the invention containing the benzimidazole and indazole heterocyclic, has good biological activity, and contain the large conjugated system, the molecule more stable. (by machine translation)

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Related Products of 38385-95-4, you can also check out more blogs about38385-95-4

Reference:
Piperidine – Wikipedia,
Piperidine | C5H14718N – PubChem