Comparing the anion binding of 4-amido- with 4-amino-1,8-naphthalimides was written by Filiti, Jacob;Hearn, Kyle;Rudebeck, Elley;Ngo, Huynh Thien;Pham-Tran, Nguyen-Nguyen;Pfeffer, Frederick. And the article was included in Organic & Biomolecular Chemistry in 2021.Application of 109-85-3 The following contents are mentioned in the article:
The synthesis and evaluation of a new anion receptor based on the 4-amido-1,8-naphthalimide scaffold is described. The findings indicate that the amide N-H is an enhanced H-bond donor but is otherwise restricted in its ability to participate in the binding of simple anions. This study involved multiple reactions and reactants, such as 2-Methoxyethylamine (cas: 109-85-3Application of 109-85-3).
2-Methoxyethylamine (cas: 109-85-3) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Application of 109-85-3
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem