Can You Really Do Chemisty Experiments About 5-Chloro-3-phenylbenzo[c]isoxazole

COA of Formula: https://www.ambeed.com/products/719-64-2.html, This is the end of this tutorial post, and I hope it has helped your research about 719-64-2.

New discoveries in chemical research and development in 2021.COA of Formula: https://www.ambeed.com/products/719-64-2.html, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction. 719-64-2, Name is 5-Chloro-3-phenylbenzo[c]isoxazole, molecular formula is C13H8ClNO. In an article, author is Chen, Cheng-yi,once mentioned of 719-64-2.

A divergent and regioselective synthesis of either 3-substituted benzisoxazoles or 2-substituted benzoxazoles from readily accessible ortho-hydroxyaryl N-H ketimines is described. The reaction proceeds in two distinct pathways through a common N-Cl imine Intermediate: (a) N-O bond formation to form benzisoxazole under anhydrous conditions and (b) NaOCl mediated Beckmann-type rearrangement to form benzoxazole, respectively. The reaction path also depends on the electronic nature of the aromatic ring, with the electron-rich aromatic rings favoring the rearrangement and the electron-deficient rings favoring the N-O bond formation. A Beckmann-type rearrangement mechanism via net [1,2]-aryl migration for the formation of 2-substituted benzoxazole is proposed.

COA of Formula: https://www.ambeed.com/products/719-64-2.html, This is the end of this tutorial post, and I hope it has helped your research about 719-64-2.

Reference:
Benzisoxazole – Wikipedia,
,Benzisoxazole – an overview | ScienceDirect Topics