Vydzhak, Roman N. et al. published their research in Molecular Diversity in 2022 | CAS: 109-85-3

2-Methoxyethylamine (cas: 109-85-3) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Name: 2-Methoxyethylamine

Rapid synthetic approaches to libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones and 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-ones was written by Vydzhak, Roman N.;Panchishin, Svitlana Ya.;Kachaeva, Maryna V.;Pilyo, Stepan G.;Moskvina, Viktoriia S.;Shablykina, Olga V.;Kozytskiy, Andriy V.;Brovarets, Volodymyr S.. And the article was included in Molecular Diversity in 2022.Name: 2-Methoxyethylamine The following contents are mentioned in the article:

An efficient and practical synthetic procedure for libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones I [R =H, 6,7-di-Me, 7-F, etc.; R1 = n-Pr, CH2CH2OH, 2-furylmethyl, etc.; Ar = Ph, 4-MeC6H4, 3,4,5-tri-MeOC6H2, etc.] using a multicomponent process was presented. A convenient synthetic procedure for obtaining functionalized 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-ones II [R2 = H, 3,5-di-Me, 4-Me-5-Cl, etc.; R3 = 4-BrC6H4, 2-OHC6H4, 3-MeO-4-OHC6H3, etc.; R4 = n-Pr, CH2CH2OH, 2-ClC6H4CH2, etc.] via ring-opening strategy was developed. This protocol was found to be compatible with a wide range of substituents and paves the way for the practical synthesis of title compounds with a broad range of substituents under mild condition. The products could be easily isolated by crystallization without the use of chromatog. This study involved multiple reactions and reactants, such as 2-Methoxyethylamine (cas: 109-85-3Name: 2-Methoxyethylamine).

2-Methoxyethylamine (cas: 109-85-3) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Name: 2-Methoxyethylamine

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem