Synthetic Route of 6249-56-5, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.6249-56-5, Name is 3-Carboxy-N,N,N-trimethylpropan-1-aminium chloride, molecular formula is C7H16ClNO2. In a Article，once mentioned of 6249-56-5
The mechanism of the pyrolysis reaction of carpronium chloride <(CH3)3N+-(CH2)3-COOCH3Cl-> leading to gamma-butyrolactone and tetramethylammonium chloride was investigated by means of thermal analysis, pyrolysis gas chromatography mass spectrometry and field desorption mass spectrometry, using deuterium labelling.The results indicated that carpronium chloride pyrolysed to yield equimolar amounts of gamma-butyrolactone and tetramethylammonium chloride, methyl transfer occured between N and O during the pyrolysis process.The mechanism is discussed on the basis of the experimental results, and with the aid of the theoretical results calculated by the CNDO/2 method.The mechanism presented is as follows. gamma-Butyrolactone is formed by the intramolecular migration of the ?-orbital of C=O to the carbon adjacent to <(CH3)3N>+ via a 5-membered ring transition state, accompained by a bimolecular reaction between <(CH3)3N>+ and the CH3 of O-CH3, resulting in the formation of tetramethylammonium chloride in an amount equimolar with gamma-butyrolactone.
The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 6249-56-5 is helpful to your research. Synthetic Route of 6249-56-5
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI