Infrared spectra of some compounds of pharmaceutical interest was written by Sammul, Oscar R.;Brannon, Wilson L.;Hayden, Alma L.. And the article was included in Journal of the Association of Official Agricultural Chemists in 1964.Application In Synthesis of 3-Methyl-4-nitroanisole This article mentions the following:
IR absorption spectra of new and nonofficial drugs, U.S.P. and N.F. items, solvents, and reagents are presented to supplement previously published spectra of U.S.P. and N.F. Reference Standards (CA 58, 3823g). In the experiment, the researchers used many compounds, for example, 3-Methyl-4-nitroanisole (cas: 5367-32-8Application In Synthesis of 3-Methyl-4-nitroanisole).
3-Methyl-4-nitroanisole (cas: 5367-32-8) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. But on the other hand, ethers undergo cleavage by reaction with acids. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Application In Synthesis of 3-Methyl-4-nitroanisole
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem