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. 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.Application of 5367-32-8
Efficient cosubstrate enzyme pairs for sequence-specific methyltransferase-directed photolabile caging of DNA was written by Heimes, Michael;Kolmar, Leonie;Brieke, Clara. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2018.Application of 5367-32-8 This article mentions the following:
Supplemented with synthetic surrogates of their natural cosubstrate S-adenosyl-L-methionine (AdoMet), methyltransferases represent a powerful toolbox for the functionalization of biomols. By employing novel cosubstrate derivatives in combination with protein engineering, we show that this chemo-enzymic method can be used to introduce photolabile protecting groups into DNA even in the presence of AdoMet. This approach enables optochem. control of gene expression in a straight-forward manner and we have termed it reversible methyltransferase directed transfer of photoactivatable groups (re-mTAG). In the experiment, the researchers used many compounds, for example, 3-Methyl-4-nitroanisole (cas: 5367-32-8Application of 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. 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.Application of 5367-32-8
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem