Morimoto, Hiroshi et al. published their research in Chemical & Pharmaceutical Bulletin in 1985 | CAS: 37905-02-5

(2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.COA of Formula: C12H18O3

Ubiquinone and related compounds. XXXVIII. Biological oxidation of ubiquinone was written by Morimoto, Hiroshi;Kurimoto, Kuniko;Imada, Isuke. And the article was included in Chemical & Pharmaceutical Bulletin in 1985.COA of Formula: C12H18O3 The following contents are mentioned in the article:

Ubiquinone-2 (I) was oxidized to 6-[7-carboxy-3-methyl-(2E,6E)-2,6-octadienyl]-2,3-dimethoxy-5-methyl-1,4-benzoquinone and 6-[6,7-dihydroxy-3,7-dimethyl-(E)-2-octenyl]-2,3-dimethoxy-5-methyl-1,4-benzoquinone by the 6000-g supernatant of guinea pig liver homogenate in the presence of NAD and NADPH-generating systems. This study involved multiple reactions and reactants, such as (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5COA of Formula: C12H18O3).

(2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.COA of Formula: C12H18O3

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics