Final Thoughts on Chemistry for tert-Butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate

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.name: tert-Butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate, you can also check out more blogs about236406-33-0

Chemistry is traditionally divided into organic and inorganic chemistry. name: tert-Butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate. The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent,Which mentioned a new discovery about 236406-33-0

The invention relates to compounds represented by the general formula [I] STR1 [wherein Ar means an aryl group or a heteroaryl group which may have a substitutive group selected from a group consisting of a halogen atom, a lower alkyl group and a lower alkoxy group; R 1 means a C 3-C 6 cycloalkyl group which is substitutable with a fluorine atom; R 2 and R 4 mean hydrogen atoms, groups represented by–(A 1) m–NH–B or the like; R. sup.3 and R 5 mean hydrogen atoms, C 1-C 6 aliphatic hydrocarbon groups or the like which are substitutable with a lower alkyl group(s); n means 0 or 1; and X means an oxygen atom or a sulfur atom].

Compounds according to the invention, since they not only have potent selective antagonistic activity against muscarinic M 3 receptors but also exhibit excellent oral activity, durability of action and pharmacokinetics, are very useful as safe and effective remedies against respiratory, urinary and digestive diseases with little adverse side effects.

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.name: tert-Butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate, you can also check out more blogs about236406-33-0

Reference:
Piperidine – Wikipedia,
Piperidine | C5H20247N – PubChem