Synthetic Route of C9H16O2. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. 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.
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.
In addition to the literature in the link below, there is a lot of literature about this compound(2,6-Dimethyl-3,5-heptanedione)Synthetic Route of C9H16O2, illustrating the importance and wide applicability of this compound(18362-64-6).
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica