Synthesis and structure of 3-isoquinolinols was written by Simchen, Gerhard;Haefner, Manfred. And the article was included in Justus Liebigs Annalen der Chemie in 1975.COA of Formula: C8H9NO3 This article mentions the following:
The isoquinolinols I (X = Cl, Br, or iodine; R = H, Cl, Br, Me, or OMe; R1 = H, Me, or OMe) were prepared by cyclization of 3,4,6-RR1(NC)C6H2CH2COCl in the presence of anhydrous HX. Hydrogenation of I over Pd/C gave I (X = H). The lactam-lactim tautomerism of these compounds was discussed. 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. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. 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.COA of Formula: C8H9NO3
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem