Litvinenko, L. M. et al. published their research in Zhurnal Organicheskoi Khimii in 1983 | CAS: 54916-28-8

1-(4-(4-Methoxyphenoxy)phenyl)ethanone (cas: 54916-28-8) 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. 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).Name: 1-(4-(4-Methoxyphenoxy)phenyl)ethanone

Synthesis and reactivity of (aryloxy)cumyl chlorides was written by Litvinenko, L. M.;Benndorf, Werner;Popova, R. S.;Popov, A. F.;Tormosin, I. I.. And the article was included in Zhurnal Organicheskoi Khimii in 1983.Name: 1-(4-(4-Methoxyphenoxy)phenyl)ethanone This article mentions the following:

Ullmann condensation of RC6H4OH (R = 3-Cl, 3-F, 4-Cl, 4-F, H, 4-Me, 4-MeO) with 4-BrC6H4COMe at 200° gave the corresponding RC6H4OC6H4COMe-4, Grignard methylation of which gave 56.1-92.9% RC6H4OC6H4CMe2OH-4 (I). Saturating the unstable I in CH2Cl2 with dry HCl gave the title chlorides, the solvolysis rates of which in 90% aqueous Me2CO increased in the stated order of R and correlated with the σ0 and σR+ constants of R (ρ0 = -1.22). In the experiment, the researchers used many compounds, for example, 1-(4-(4-Methoxyphenoxy)phenyl)ethanone (cas: 54916-28-8Name: 1-(4-(4-Methoxyphenoxy)phenyl)ethanone).

1-(4-(4-Methoxyphenoxy)phenyl)ethanone (cas: 54916-28-8) 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. 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).Name: 1-(4-(4-Methoxyphenoxy)phenyl)ethanone

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