2-(4-Methoxyphenoxy)acetohydrazide was written by Liu, Gang;Gao, Jie. And the article was included in Acta Crystallographica, Section E: Structure Reports Online in 2012.Application In Synthesis of 2-(4-Methoxyphenoxy)acetic acid This article mentions the following:
The title compound, C9H12N2O3, was synthesized by the reaction of Et 2-(4-methoxyphenoxy)acetate with hydrazine hydrate in ethanol. In the acetohydrazide group, the N-N bond is relatively short [1.413 (2) Å], suggesting some degree of electronic delocalization in the mol. In the crystal, mols. are linked into sheets lying parallel to the ab plane by N-H···N and N-H···O hydrogen bonds. Crystallog. data are given. In the experiment, the researchers used many compounds, for example, 2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4Application In Synthesis of 2-(4-Methoxyphenoxy)acetic acid).
2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4) 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, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil. 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 2-(4-Methoxyphenoxy)acetic acid
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem