Cyclobutane-bicyclobutane systems. 11. Formation and stability of alkoxyimidates in the cyclobutane-bicyclobutane system was written by Hoz, S.;Aurbach, D.. And the article was included in Tetrahedron in 1985.Safety of Methyl 3,3-dimethoxycyclobutanecarboxylate This article mentions the following:
Reactions of CN– with the bicyclobutane derivatives I and II (X = Cl, Br) in MeOH gave the alkoxyimidates, for which equilibrium formation constants were determined Imidate formation was favored by electron-withdrawing groups. The central bond of the bicyclobutane moiety was a good mediator for transmitting electronic effects. In the experiment, the researchers used many compounds, for example, Methyl 3,3-dimethoxycyclobutanecarboxylate (cas: 98231-07-3Safety of Methyl 3,3-dimethoxycyclobutanecarboxylate).
Methyl 3,3-dimethoxycyclobutanecarboxylate (cas: 98231-07-3) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. 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.Safety of Methyl 3,3-dimethoxycyclobutanecarboxylate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics