Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Analytica Chimica Acta called Effect of substituents on the distribution coefficients of alkyl-substituted β-diketones and their copper and iron chelates, Author is Koshimura, Hideo; Okubo, Teiji, which mentions a compound: 18362-64-6, SMILESS is CC(C)C(CC(C(C)C)=O)=O, Molecular C9H16O2, Reference of 2,6-Dimethyl-3,5-heptanedione.
A series of alkyl-substituted β-diketones consisting of acetylacetone, dipropionylmethane, diisobutyrylmethane, dipivaloylmethane, dibutyrylmethane, divalerylmethane, dicaproylmethane and diisovalerylmethane was studied to establish the effect of substituents on the extraction constants and the acid dissociation constants The logarithm of the distribution coefficients of the β-diketones and of their Cu(II) and Fe(III) chelates was a linear function of the number of C atoms in the mol. The distribution coefficient increased by a factor of 4 for each addnl. C atom.
In addition to the literature in the link below, there is a lot of literature about this compound(2,6-Dimethyl-3,5-heptanedione)Reference of 2,6-Dimethyl-3,5-heptanedione, illustrating the importance and wide applicability of this compound(18362-64-6).
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica