3,7-Dioxaazelaamides as ionophores for lithium ion selective liquid membrane electrodes was written by Metzger, Erich;Aeschimann, Roland;Egli, Martin;Suter, Gaby;Dohner, Rene;Ammann, Daniel;Dobler, Max;Simon, Wilhelm. And the article was included in Helvetica Chimica Acta in 1986.Category: alcohols-buliding-blocks The following contents are mentioned in the article:
Neutral lipophilic dioxaazelaamides I (R = H, Me, CMe2; R1 = H, Me, Et; R2 = H, Me, Bu) were prepared and incorporated in lipophilic liquid membranes. Li+-Na+ selectivities of these were ≤80; the membranes allow reliable measurements of Li+ in blood serum within the clin. concentration range. The structure of the LiSCN complex with I (R = H; R1 = R2 = Me) was determined by x-ray crystallog. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Category: alcohols-buliding-blocks).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Category: alcohols-buliding-blocks
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts