Easy and mild fluoride-mediated direct mono- and dialkoxylation of perylenediimides was written by Zink-Lorre, Nathalie;Font-Sanchis, Enrique;Sastre-Santos, Angela;Fernandez-Lazaro, Fernando. And the article was included in Dyes and Pigments in 2016.Related Products of 110590-84-6 This article mentions the following:
The reaction of perylenediimides with alcs. in the presence of fluoride anions yields 1-alkoxy- or 1,6(7)-dialkoxyperylenediimides under very mild metal-free conditions. The reaction can also be applied to bay- and ortho-brominated perylenediimides. In the experiment, the researchers used many compounds, for example, 2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d’e’f’]diisoquinoline-1,3,8,10(2H,9H)-tetraone (cas: 110590-84-6Related Products of 110590-84-6).
2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d’e’f’]diisoquinoline-1,3,8,10(2H,9H)-tetraone (cas: 110590-84-6) belongs to isoquinoline derivatives. Quinoline is a catabolite of tryptophan, the basic structure of some antihypertensive drugs, such as the peripheral vasodilators prazosin and doxazosin. Most traditional methods of generating isoquinoline do so via oxidative aromatization of dihydro- or tetrahydro-isoquinolines, usually offering some environmental or economic advantage.Related Products of 110590-84-6
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem