Awesome Chemistry Experiments For 5-Nitro-2,3-dihydro-1,3-benzoxazol-2-one

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Reference of 3889-13-2. In my other articles, you can also check out more blogs about 3889-13-2

Reference of 3889-13-2, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Article, and a compound is mentioned, 3889-13-2, 5-Nitro-2,3-dihydro-1,3-benzoxazol-2-one, introducing its new discovery.

The vicarious nucleophilic substitution of hydrogen and related reactions in nitrobenzoxazoles

5- and 6-nitrobenzoxazoles 3 and 4 react with nucleophiles exclusively at C-2, giving ring opening products. If position 2- is blocked with phenyl substituent the reaction takes place in the carbocyclic ring affording the VNS products. 2-Methylthio-5-nitrobenzoxazole 7 and its 6-nitro isomer 8 give products which result from addition of a nucleophile to the carbocyclic ring (VNS) as well as to the heterocyclic ring (S(N)Ar and ring cleavage). 2-Methylthiobenzoxazoles can be readily converted to the corresponding benzoxazolones via oxidative hydrolysis.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Reference of 3889-13-2. In my other articles, you can also check out more blogs about 3889-13-2

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