Nametkin, N. S. et al. published their research in Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya in 1982 | CAS: 5388-42-1

2-Phenylisoindolin-1-one (cas: 5388-42-1) belongs to indole derivatives. Indole exists overwhelmingly in the 1H-indole form as do other simple indoles. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Name: 2-Phenylisoindolin-1-one

Action of sulfur on μ-[(o-phenylenemethylene)(phenylamino)]diiron hexacarbonyl was written by Nametkin, N. S.;Tyurin, V. D.;Nekhaev, A. I.;Kondrat’eva, M. G.;Sobolev, Yu. P.. And the article was included in Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya in 1982.Name: 2-Phenylisoindolin-1-one This article mentions the following:

The title reaction in C6H6 at 80° gave S2Fe2(CO)6 12, S2Fe3(CO)9 3, I 6, II 33, PhCH(NHPh)2 11, Ph3N 2, III 11, and PhNH2 22%. In the experiment, the researchers used many compounds, for example, 2-Phenylisoindolin-1-one (cas: 5388-42-1Name: 2-Phenylisoindolin-1-one).

2-Phenylisoindolin-1-one (cas: 5388-42-1) belongs to indole derivatives. Indole exists overwhelmingly in the 1H-indole form as do other simple indoles. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Name: 2-Phenylisoindolin-1-one

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