Islam, Nurul et al. published their research in Bangladesh Journal of Scientific and Industrial Research in 1992 | CAS: 5367-32-8

3-Methyl-4-nitroanisole (cas: 5367-32-8) 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. Autoxidation is the spontaneous oxidation of a compound in air. In the presence of oxygen, ethers slowly autoxidize to form hydroperoxides and dialkyl peroxides. If concentrated or heated, these peroxides may explode. To prevent such explosions, ethers should be obtained in small quantities, kept in tightly sealed containers, and used promptly.COA of Formula: C8H9NO3

Reductions of disubstituted nitrobenzenes with metal hydrides. Part II. Use of sodium borohydride in the preparation of tetrasubstituted azoxybenzenes was written by Islam, Nurul;Khan, Abdus Samad. And the article was included in Bangladesh Journal of Scientific and Industrial Research in 1992.COA of Formula: C8H9NO3 This article mentions the following:

Five azoxybenzenes X(Me)C6H4N(O):NC6H4(Me)X (X = halide) were prepared in 80-90% yield by reduction of halo(methyl)nitrobenzenes with NaBH4 in EtOH or MeOH. Nitrobenzenes containing an o– or p-fluoride relative to the nitro group were not reduced; rather, the F was replaced by alkoxide from the solvent. Oxidation of dihalodimethylazobenzenes X(Me)C6H4N:NC6H4(Me)X with AcOOH (30% H2O2 in AcOH) afforded 8 tetrasubstituted azoxybenzenes in 83-88% yield. Reduction of the azoxybenzenes with Zn dust and AcOH gave the corresponding azobenzenes. In the experiment, the researchers used many compounds, for example, 3-Methyl-4-nitroanisole (cas: 5367-32-8COA of Formula: C8H9NO3).

3-Methyl-4-nitroanisole (cas: 5367-32-8) 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. Autoxidation is the spontaneous oxidation of a compound in air. In the presence of oxygen, ethers slowly autoxidize to form hydroperoxides and dialkyl peroxides. If concentrated or heated, these peroxides may explode. To prevent such explosions, ethers should be obtained in small quantities, kept in tightly sealed containers, and used promptly.COA of Formula: C8H9NO3

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