Carbolines. Part VII. Anisidines, convenient tools to synthesize hydroxy-灏?carbolines was written by Rocca, Patrick;Marsais, Francis;Godard, Alain;Queguiner, Guy;Adams, Luqman;Alo, Babajide. And the article was included in Journal of Heterocyclic Chemistry in 1995.HPLC of Formula: 56619-93-3 This article mentions the following:
The paper describes a convenient synthesis of hydroxy-灏?carbolines from com. anisidines based on key steps such as metalation, cross-coupling and cyclization. The first total synthesis of a major cytotoxic constituent of a marine bryozoan is also reported, the 8-hydroxy-1-vinyl-灏?carboline. In the experiment, the researchers used many compounds, for example, N-(3-Methoxyphenyl)pivalamide (cas: 56619-93-3HPLC of Formula: 56619-93-3).
N-(3-Methoxyphenyl)pivalamide (cas: 56619-93-3) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. But ether is more polar than alkenes. At room temperature, ethers are pleasant-smelling colourless liquids. 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.HPLC of Formula: 56619-93-3
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem