Name: 2,6-Dimethyl-3,5-heptanedione. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 2,6-Dimethyl-3,5-heptanedione, is researched, Molecular C9H16O2, CAS is 18362-64-6, about Asymmetrically modified Raney nickel catalyst (MRNi). Preparation of highly active new catalyst and its applications. Author is Tai, Akira; Kikukawa, Tadasi; Sugimura, Takasi; Inoue, Yoshihisa; Osawa, Tsutomu.
Tartaric acid-NaBr-modified Raney nickel catalyst was prepared from ultrasonicated Raney nickel catalyst. This catalyst (TA-NaBr-MRNi-U) showed high hydrogenation activity in the enantiodifferentiating hydrogenation of Me acetoacetate and its homologs, acetylacetone, and 2,6-dimethyl-3,5-heptanedione. From the hydrogenation products, optically pure 3-hydroxybutanic acid and its homologs, 2,4-pentanediol, and 2,6-dimethyl-3,5-heptanediol, were obtained in excellent yield.
Although many compounds look similar to this compound(18362-64-6)Name: 2,6-Dimethyl-3,5-heptanedione, numerous studies have shown that this compound(SMILES:CC(C)C(CC(C(C)C)=O)=O), has unique advantages. If you want to know more about similar compounds, you can read my other articles.
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica