Awesome and Easy Science Experiments about 5-Nitro-2,3-dihydro-1,3-benzoxazol-2-one

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 3889-13-2

Electric Literature of 3889-13-2, 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.3889-13-2, Name is 5-Nitro-2,3-dihydro-1,3-benzoxazol-2-one, molecular formula is C7H4N2O4. In a article£¬once mentioned of 3889-13-2

A Simple Synthesis of 2(3H)-Benzoxazolones using Phenyl Chloroformate

2(3H)-Benzoxazolones 3 can be prepared directly from the corresponding 2-aminophenols and phenyl chloroformate.The intermediate 2-hydroxy phenylcarbamates 2 are formed easily in aqueous alcohol solvent and these are converted rapidly to product, without their isolation, using one equivalent of sodium hydroxide.The synthesis accommodates a wide variety of substituents, including the easily hydrolyzed ethyl ester.

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 3889-13-2

Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem