Flash vacuum pyrolysis of some N-benzylbenzotriazoles and N-benzylbenzisoxazolones was written by Khalafy, Jabbar;Prager, Rolf H.. And the article was included in Australian Journal of Chemistry in 1998.HPLC of Formula: 5388-42-1 This article mentions the following:
The flash vacuum pyrolysis products of 2-(benzotriazol-1-ylmethyl)benzonitrile, Me 2-(benzotriazol-1-ylmethyl)benzoate, and the corresponding benzisoxazolones have been characterized. The benzotriazoles lose nitrogen to give diradicals, which undergo intramol. hydrogen-atom transfer or cyclization, while the benzisoxazolones rearrange initially to the corresponding benzaldehyde N-(2-carboxyphenyl)imines, which undergo subsequent intramol. addition reactions. In the experiment, the researchers used many compounds, for example, 2-Phenylisoindolin-1-one (cas: 5388-42-1HPLC of Formula: 5388-42-1).
2-Phenylisoindolin-1-one (cas: 5388-42-1) belongs to indole derivatives. Indole, also called Benzopyrrole, a heterocyclic organic compound occurring in some flower oils, such as jasmine and orange blossom, in coal tar, and in fecal matter. Moreover, it is known that it controls biofilm formation. However, the role of indole in the cell has not been fully elucidated.HPLC of Formula: 5388-42-1
Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles