Synthesis of Unsymmetrical Vicinal Diamines via Directed Hydroamination was written by Lee, Byung Joo;Ickes, Andrew R.;Gupta, Anil K.;Ensign, Seth C.;Ho, Tam D.;Tarasewicz, Anika;Vanable, Evan P.;Kortman, Gregory D.;Hull, Kami L.. And the article was included in Organic Letters in 2022.Quality Control of 2-Methoxyethylamine The following contents are mentioned in the article:
The rhodium-catalyzed hydroamination of primary and secondary allylic amines using diverse amine nucleophiles, including primary, secondary, acyclic, and cyclic aliphatic amines to access a wide range of unsym. vicinal diamines, was presented. The utility of this methodol. was further demonstrated through the rapid synthesis of several bioactive mols. and analogs. This study involved multiple reactions and reactants, such as 2-Methoxyethylamine (cas: 109-85-3Quality Control of 2-Methoxyethylamine).
2-Methoxyethylamine (cas: 109-85-3) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Quality Control of 2-Methoxyethylamine
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem