Chen, Ling Ching et al. published their research in Journal of the Chinese Chemical Society (Taipei, Taiwan) in 1984 | CAS: 56619-93-3

N-(3-Methoxyphenyl)pivalamide (cas: 56619-93-3) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive. Ethers can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds.Application In Synthesis of N-(3-Methoxyphenyl)pivalamide

Synthesis of 5-(3-tert-butylamino-2-hydroxy)propoxy-3,4-dihydrocarbostyril. was written by Chen, Ling Ching;Lin, Jen Hom;Wu, Shihn Sheng. And the article was included in Journal of the Chinese Chemical Society (Taipei, Taiwan) in 1984.Application In Synthesis of N-(3-Methoxyphenyl)pivalamide This article mentions the following:

The title compound ( carteolol, I) was prepared in 21% yield in 6 steps from m-Me3CCOC6H4OMe via cyclization of the amino ester II to the carbostyril III. In the experiment, the researchers used many compounds, for example, N-(3-Methoxyphenyl)pivalamide (cas: 56619-93-3Application In Synthesis of N-(3-Methoxyphenyl)pivalamide).

N-(3-Methoxyphenyl)pivalamide (cas: 56619-93-3) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive. Ethers can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds.Application In Synthesis of N-(3-Methoxyphenyl)pivalamide

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