Reference of 89424-83-9, 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.89424-83-9, Name is 1,3-Dihydroisobenzofuran-5-carbaldehyde, molecular formula is C9H8O2. In a article，once mentioned of 89424-83-9
A short and versatile synthesis of alpha,beta-dibenzyl-gamma-butyrolactones has been developed starting from inexpensive materials by applying Stobbe condensation and following the novel reductive cyclisation with sodiumborohydride. Natural products Suchilactone (5a), Kaerophyllin (5b), savinin (5d) and anhydropodorhizol (5f) were prepared in racemic form. New thionolactones (6a?6e) were prepared by treating these lignans with Lawesson?s reagent. For all the prepared compounds the antioxidant, anti-inflammatory (5-lipoxygenase inhibition) and cytotoxic (Brine shrimp lethality test) activities were tested. The compounds 5a, 5b, 5c, 5d, 5e and 5f showed good 5-lipoxygenase inhibition activity. The thiono lignan 6d showed impressive cytotoxic activity.
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 89424-83-9