Synthetic Route of 1123-49-5, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1123-49-5, Name is 3,5-Dimethyl-4-nitroisoxazole, molecular formula is C5H6N2O3. In a Article，once mentioned of 1123-49-5
Synthesis of functionalized isoxazole-oxindole hybrids via on water, catalyst free vinylogous Henry and 1,6-Michael addition reactions
Various 3-substituted-3-hydroxy isoxazole-oxindole hybrids were synthesized via the vinylogous Henry reaction of 3,5-dimethyl-4-nitroisoxazole and isatin using water as a reaction medium under catalyst free conditions at 50 C. Systematic studies were carried out to understand the role of the water on the reaction by using D2O, brine, ethylene glycol and PEG-400 as a reaction medium along with organic solvents. Among all of these, water (0.170 mol concentration) was found be more efficient giving desired products in 82-99% yields in 45-120 min. Further the quaternary centre (3 alcohol) generated was used for the creation of a double bond which was again used for a 1,6-Michael reaction to produce highly functionalized isoxazole-oxindole derivatives.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 1123-49-5. In my other articles, you can also check out more blogs about 1123-49-5
Reference：
Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem