Inoue, Seiichi et al. published their research in Chemistry Letters in 1986 | 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 perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. 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.Recommanded Product: (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate

Regio- and stereoselective oxidation of gem-dimethyl olefins via [2,3]-sigmatropic rearrangement of allyl amine oxides was written by Inoue, Seiichi;Iwase, Norimichi;Miyamoto, Osamu;Sato, Kikumasa. And the article was included in Chemistry Letters in 1986.Recommanded Product: (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate The following contents are mentioned in the article:

Highly regio- and stereoselective oxidation sequences are described for the efficient conversion of the gem-di-Me alkene terminus of acyclic terpenes to terminal trans-allylic alcs. and trans-α,β-unsaturated aldehydes. Thus, chlorination of CH2:CMeCH2R (R = CH2CMe:CHCH2OCH2Ph) by Ca(OCl)2 in CH2Cl2-H2O containing dry ice, followed by amination with Me2NH, gave CH2:CMeCH(NMe2)R, which underwent oxidation with AcOOH to give the N-oxide; this, when treated with Zn in aqueous AcOH, gave quant. HOCH2CMe:CHCH2R. Treating the N-oxide with R1X (R1 = Me, allyl) in refluxing CHCl3 gave quant. RCH2CH:CMeCHO. This study involved multiple reactions and reactants, such as (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5Recommanded Product: (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate).

(2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. 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.Recommanded Product: (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate

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