A new application about 2-(Piperidin-4-yl)-1H-benzo[d]imidazole

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 38385-95-4

Synthetic Route of 38385-95-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.38385-95-4, Name is 2-(Piperidin-4-yl)-1H-benzo[d]imidazole, molecular formula is C12H15N3. In a Article，once mentioned of 38385-95-4

Procedures are described for the preparation of various bidentate and potentially tridentate chelating agents.These incorporate pyridyl, benzimidazole, imidazole or phenolic moieties.Phillips condensations of carboxylic acids with o-phenylenediamines were carried out in 4 M hydrochloric acid.Syntheses are reported for 2,6-bis(N’-methylimidazol-2′-ylthiomethyl)pyridine, 2,6-bis(benzimidazol-2′-ylthiomethyl)pyridine, 2-(4′-piperidyl)benzimidazole, 2-(3′-piperidyl)benzimidazole, 2-(3-N’-methylpiperidyl)benzimidazole, 2-(3-N’-methylpiperidyl)-N-methylbenzimidazole, 2-(2′-hydroxybenzyl)benzimidazole and 2-(2′-hydroxybenzyl)-N-methylbenzimidazole.The compounds were characterized where appropriate by their mass, uv, and 1H-nmr spectra. 2-(2′-Hydroxybenzyl)benzimidazole hydrochloride acts as a gelling agent in aqueous solution.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 38385-95-4

Reference：
Piperidine – Wikipedia,
Piperidine | C5H14731N – PubChem