Quality Control of 2,6-Dimethyl-3,5-heptanedione. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 2,6-Dimethyl-3,5-heptanedione, is researched, Molecular C9H16O2, CAS is 18362-64-6, about H2O2-mediated oxidative formation of amides from aromatic amines and 1,3-diketones as acylation agents via C-C bond cleavage at room temperature in water under metal-free conditions. Author is Sun, Xi; Wang, Min; Li, Pinhua; Zhang, Xiuli; Wang, Lei.
1,3-Diketones, as novel acylation agents, reacted with aromatic amines promoted by com. available H2O2 (30% aqueous) as the sole oxidant at room temperature under metal-free conditions in water, leading to a novel and rapid amide bond formation strategy. The reported method is high-yielding, simple and mild, and is the first example of the use of 1,3-diketones as acylation agents via C-C bond cleavage.
As far as I know, this compound(18362-64-6)Quality Control of 2,6-Dimethyl-3,5-heptanedione can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica