3D-TAA10229 - 2-methyl-6-nitroanisole

2-Methyl-5-nitroanisole is a phenol that can be synthesized by the demethylation of 2,6-dichlorophenol with tribromide. It can also be synthesized from benzaldehyde and benzoic acid. 2-Methyl-5-nitroanisole has been used as a cardiotonic for its ability to increase the strength of heart contractions. It also has been shown to be an intermediate in the synthesis of boron compounds. This compound is fluorinated and yields high yields when synthesized from benzaldehyde and benzoic acid. 2-Methyl-5-nitroanisole is a nucleophile that reacts with electrophiles such as amines, thiols, sulfides, alcohols, and carboxylic acids.

1-Methoxy-2-methyl-3-nitrobenzene

3-Methyl-2-nitroanisole is a synthetic monosubstituted nitro compound that can be produced by the oxidation of 3,4-dimethoxybenzaldehyde. It has three methyl groups and one nitro group on its ring. 3-Methyl-2-nitroanisole has been used in high concentrations as a reactant for the synthesis of other compounds. It can also be used to synthesize anthranilic acid, which is an intermediate in the synthesis of many dyes and pharmaceuticals. 3-Methyl-2-nitroanisole has been characterized using vibrational spectroscopy and NMR spectroscopy with frequency values ranging from 9 to 22 cm/sec, depending on substituents. The molecular weight is estimated at 196 g/mol. 3MNA has been shown to undergo demethylation and hydrolysis under acidic conditions to produce 2,5-dihydroxyanth

2-Methyl-3-nitroanisole is a synthetic molecule with a bicyclic, cyclized ring system. It was synthesized by the cyclization reaction of 2-methylbenzaldehyde and nitroethane. The reductive amination of 2-methyl-3-nitroanisole with hydroxylamine yields a mixture of products that can be used to study intramolecular reductive amination.