Qian, Guo-hua et al. published their research in Beijing Ligong Daxue Xuebao in 2001 | CAS: 1132-95-2

1,1-Diisopropoxycyclohexane (cas: 1132-95-2) 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).SDS of cas: 1132-95-2

Alkoxylation protection for hydroxy of erythromycin oxime was written by Qian, Guo-hua;Shi, Yan;Sun, Jing-guo;Yao, Guo-wei. And the article was included in Beijing Ligong Daxue Xuebao in 2001.SDS of cas: 1132-95-2 This article mentions the following:

The reaction of dialkyloxy cyclohexane with erythromycin oxime was studied. Exptl. results show that 1,1-diisopropyloxy cyclohexenane and 1,1-diethoxy cyclohexenane can be considered as protective reagents for hydroxy of erythromycin oximes. The optimal reaction conditions are as follows: reaction solvent: dichloromethane; catalyst: pyridine hydrochloride; reaction temperature: 40°C: reaction time: 1 h to 7 h. In the experiment, the researchers used many compounds, for example, 1,1-Diisopropoxycyclohexane (cas: 1132-95-2SDS of cas: 1132-95-2).

1,1-Diisopropoxycyclohexane (cas: 1132-95-2) 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).SDS of cas: 1132-95-2

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