The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 2,6-Dimethyl-3,5-heptanedione, is researched, Molecular C9H16O2, CAS is 18362-64-6, about Metal- and Oxidant-Free Synthesis of Quinazolinones from β-Ketoesters with o-Aminobenzamides via Phosphorous Acid-Catalyzed Cyclocondensation and Selective C-C Bond Cleavage, the main research direction is quinazolinone preparation cyclocondensation ketoester aminobenzamide carbon carbon bond cleavage; phosphorus acid catalyzed cyclocondensation quinazolinone benzimidazole benzothiazole preparation.Name: 2,6-Dimethyl-3,5-heptanedione.
A general and efficient phosphorous acid-catalyzed cyclocondensation of β-ketoesters with o-aminobenzamides via selective C-C bond cleavage leading to quinazolinones is developed. This reaction proceeds smoothly under metal- and oxidant-free conditions, giving both 2-alkyl- and 2-aryl-substituted quinazolinones in excellent yields. This strategy can also be applied to the synthesis of other N-heterocycles, such as benzimidazoles and benzothiazoles.
There is still a lot of research devoted to this compound(SMILES：CC(C)C(CC(C(C)C)=O)=O)Name: 2,6-Dimethyl-3,5-heptanedione, and with the development of science, more effects of this compound(18362-64-6) can be discovered.
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica