Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Agricultural and Biological Chemistry called Microbial degradation of nitrile compounds. Part III. Degradation of dinitriles by Fusarium merismoides TG-1, Author is Asano, Yasuhisa; Ando, Shinji; Tani, Yoshiki; Yamada, Hideaki, which mentions a compound: 4553-62-2, SMILESS is N#CC(C)CCC#N, Molecular C6H8N2, SDS of cas: 4553-62-2.
The triacrylonitrile-utilizing fungus F. merismoides TG-1 grew on a medium containing dinitriles as the N source. It degraded glutaronitrile to 4-cyanobutyric acid and diacrylonitrile to 4-cyanopentanoic acid.
If you want to learn more about this compound(2-Methylglutaronitrile)SDS of cas: 4553-62-2, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(4553-62-2).
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com