One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, name: 5-Methoxy-3,4-dihydro-2H-pyrrole, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 5264-35-7, Name is 5-Methoxy-3,4-dihydro-2H-pyrrole, molecular formula is C5H9NO
Acetylcholinesterase inhibition by fused dihydroquinazoline compounds
A new type of dihydroquinazoline-based inibitor of acetylcholinesterase (AChE) is described. These compounds were designed to interact with the catalytic site of AChE in a manner similar to the known inhibitor tacrine. In a manner analogous to the potency enhancement obtained by addition of chlorine atoms to the tacrine molecule, a 3-chloro derivative of the parent hexahydroazepino[2,1-b]quinazoline structure was found to be about 8 times more potent as an AChE inhibitor than the unsubstituted compound.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. name: 5-Methoxy-3,4-dihydro-2H-pyrrole, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 5264-35-7, in my other articles.
Reference£º
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem