Regioselective synthesis of the 4,5-dialkoxy-2-nitroanilines bearing two different alkoxy substituents was written by Grolik, Jaroslaw;Reka, Pawel;Gorczyca, Magdalena;Stadnicka, Katarzyna. And the article was included in Tetrahedron Letters in 2022.HPLC of Formula: 106-21-8 The following contents are mentioned in the article:
This article reported the regioselective and chemoselective synthesis of 4,5-dialkoxy-2-nitroanilines I [R1 = Me, Et, i-Bu, etc.; R2 = Me, i-Pr, n-Bu, etc.] substituted with two alkoxys at C-4 and C-5. Here the optimization protocol of the transetherification reaction used to synthesize 20 new compounds with good to excellent yields (50-92%) was showed. A simple and efficient one-step procedure was described that could be applied to obtain a significant number of pharmacol. active compounds, including antimalarial drug Primaquine analogs. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8HPLC of Formula: 106-21-8).
3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.HPLC of Formula: 106-21-8
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts