2-Amino-4-nitro-5-methoxybenzoic acid, with the CAS number 196194-99-7, is an organic compound characterized by its aromatic structure, which includes a benzoic acid moiety substituted with an amino group, a nitro group, and a methoxy group. This compound typically exhibits properties associated with both acidic and basic functionalities due to the presence of the carboxylic acid and amino groups. The nitro group contributes to its electron-withdrawing characteristics, which can influence its reactivity and solubility in various solvents. The methoxy group, being an electron-donating substituent, can affect the compound's overall electronic properties and steric hindrance. In terms of applications, compounds like this are often studied for their potential roles in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. Additionally, the presence of multiple functional groups allows for diverse chemical reactivity, making it a subject of interest in medicinal chemistry and material science. Safety and handling precautions should be observed, as with many nitro-substituted compounds, due to potential toxicity and environmental concerns.

2-Amino-4-nitro-5-methoxybenzoic Acid

196194-99-7: 2-Amino-5-methoxy-4-nitrobenzoic acid, Benzoic acid, 2-amino-5-methoxy-4-nitro-

2-Amino-5-methoxy-4-nitrobenzoic acid

2-Amino-4-nitro-5-methoxybenzoic acid is a chemical compound that is used in the synthesis of peptide mimetics. The presence of intramolecular hydrogen bonds and the spatial arrangement of the nitro group and methoxy group in this molecule are responsible for its intramolecular nature. When synthesized as a dimer, these two molecules form hydrogen bonds with each other. This chemical can be used to produce oligomers with conformationally restricted side chains by reacting it with an appropriate amine or alcohol.

CAS 196194-99-7: 2-Amino-4-nitro-5-methoxybenzoic Acid

2-Amino-5-methoxy-4-nitrobenzoic acid

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2-Amino-4-nitro-5-methoxybenzoic acid

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2-Amino-5-methoxy-4-nitrobenzoic acid

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