Sources of common compounds: 18362-64-6

Although many compounds look similar to this compound(18362-64-6)Recommanded Product: 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.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Palladium-Catalyzed Intramolecular Oxidative Alkylation of Unactivated Olefins, published in 2003-01-22, which mentions a compound: 18362-64-6, Name is 2,6-Dimethyl-3,5-heptanedione, Molecular C9H16O2, Recommanded Product: 2,6-Dimethyl-3,5-heptanedione.

Reaction of 5,5-dimethyl-8-nonene-2,4-dione catalyzed by PdCl2(CH3CN)2 (5 mol %) in the presence of CuCl2 (2.5 equiv) at room temperature for 3 h formed 2-acetyl-3,6,6-trimethyl-2-cyclohexenone in 96% isolated yield. Palladium-catalyzed intramol. oxidative alkylation tolerated a range of substitution and was applicable to the synthesis of spirobicyclic compounds, e.g., I, and to the cyclization of ζ-alkenyl β-keto esters.

Although many compounds look similar to this compound(18362-64-6)Recommanded Product: 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