Top Picks: new discover of Ethyl tetrahydrofuran-2-carboxylate

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. 16874-34-3, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 16874-34-3, in my other articles.

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, 16874-34-3, such as the rate of change in the concentration of reactants or products with time.In a article, authors is Mimero, mentioned the application of 16874-34-3, Name is Ethyl tetrahydrofuran-2-carboxylate, molecular formula is C7H12O3

Regioselective cleavage of tetrahydrofurans bearing proximate functional groups with acid iodides

Tetrahydrofurans functionalized at the C2 or C3 position (alcohols, esters, amine, ether, acetal) are cleaved with RCOCl/NaI (R = Me, tBu) in acetonitrile to give regioselectively trifunctionalized derivatives. In all cases the cleavage occurs mainly or exclusively at the C-O bond the most remote from the functional group.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. 16874-34-3, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 16874-34-3, in my other articles.

Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem