One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Application In Synthesis of 1-(Benzo[d]oxazol-2-yl)ethanone, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 122433-29-8, Name is 1-(Benzo[d]oxazol-2-yl)ethanone, molecular formula is C9H7NO2
Assembling heterocycle-tethered C-glycosyl and alpha-amino acid residues via 1,3-dipolar cycloaddition reactions
(Equation Presented) The 1,3-dipolar cycloadditions of C-glycosyl nitrile oxides and acetylenes to an alkyne and an azide, respectively, bearing a masked glycinyl moiety furnished disubstituted isoxazoles and triazoles. Unveiling the glycinyl group in these cycloadducts afforded C-glycosyl alpha-amino acids in which the two bioactive entities were tethered through rigid five-membered heterocycles. Optimized entries to the same compounds involved the use of unmasked but protected alkyne- and azide-containing amino acids as the partners of 1,3-dipolar cycloadditions.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Application In Synthesis of 1-(Benzo[d]oxazol-2-yl)ethanone, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 122433-29-8
Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem