Reference of 1679-47-6, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1679-47-6, Name is 3-Methyldihydrofuran-2(3H)-one, molecular formula is C5H8O2. In a article，once mentioned of 1679-47-6
Based on the most stable conformation of ZD6169, a series of N-arylated derivative of oxazolidindione (2), morpholin-3- one (3 5), piperidin-2-one (6), and pyrrolidin-2-one (7 13) was synthesized and evaluated for potassium channel opening activity. In the in-vitro assay , N-(4-benzoylphenyl)-piperidin-2-one (6) and N-(4-benzoylphenyl)-3,3-dimethyl-pyrrolidin-2-one (9) demonstrated potent and selective relaxant activity at the bladder detrusor muscle [IC50, bladder =7.4 and 6.7 muM, respectively; IC50 ratio (portal vein/bladder)=41 and 51, respectively]. Copyright
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 1679-47-6
Reference：
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem