Application of 288-14-2, 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.288-14-2, Name is Isoxazole, molecular formula is C3H3NO. In a article，once mentioned of 288-14-2
Donor-Acceptor Styrylisoxazoles: Solvatochromism and Large First Hyperpolarizability
The present work describes the synthesis and linear as well as nonlinear optical studies of donor-acceptor based styrylisoxazoles. Six styrylisoxazoles were synthesized, and examination of their photophysical properties reveals strong solvent polarity sensitivity due to intramolecular charge transfer characteristics. Most interestingly, we have measured large first hyperpolarizability (beta) values for these styrylisoxazoles. The largest beta value calculated was for the compound that bears the dimethylamine group as the donating moiety. Our current results suggest that a careful selection of the donor and acceptor groups can potentially lead to unprecedented enhancement of the (beta) values of isoxazole derivatives.
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 288-14-2
Reference：
Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem