Application of 29976-53-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.29976-53-2, Name is N-Carbethoxy-4-piperidone, molecular formula is C8H13NO3. In a Article，once mentioned of 29976-53-2
N-Substituted 4-piperidones react with beta-dimethylaminoacrolein aminals to give keto-cyanines containing a piperidine ring. A reaction of 3-dimethylamino-1, 1,3-trimethoxypropane with 1-ethoxycarbonylpiperidin-4- ylidenemalononitrile produces a cross-conjugated omega,omega?-bis- (dimethylamino) dinitrile. Its yield is doubled when ionic liquids are used. The spectroscopic properties of the compounds obtained are highly sensitive to the structure: replacement of the C=O group in ketocyanines by the C=C(CN) 2 group results in a considerable bathochromic shift of the absorption spectra, while replacement of the central bridging fragment (CH 2)3 by (CH2)4 results in a hypsochromic shift. All the compounds obtained exhibit positive solvatochromism.
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 29976-53-2
Reference：
Piperidine – Wikipedia,
Piperidine | C5H10046N – PubChem