CAS 577-72-0
:4-Methoxy-3-nitrobenzenamine
Description:
4-Methoxy-3-nitrobenzenamine, also known as p-methoxy-3-nitroaniline, is an organic compound characterized by the presence of both a methoxy group (-OCH₃) and a nitro group (-NO₂) attached to a benzene ring that also bears an amino group (-NH₂). This compound typically appears as a solid and is soluble in organic solvents. Its molecular structure features a nitro group in the meta position relative to the amino group and a methoxy group in the para position, which influences its reactivity and properties. The presence of the nitro group generally enhances the compound's electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions. Additionally, the methoxy group can affect the compound's electronic properties and solubility. 4-Methoxy-3-nitrobenzenamine is often utilized in the synthesis of dyes, pharmaceuticals, and agrochemicals, highlighting its significance in organic synthesis and industrial applications. As with many nitro compounds, it is essential to handle it with care due to potential toxicity and environmental concerns.
Formula:C7H8N2O3
InChI:InChI=1S/C7H8N2O3/c1-12-7-3-2-5(8)4-6(7)9(10)11/h2-4H,8H2,1H3
InChI key:InChIKey=RUFOHZDEBFYQSV-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(OC)C=CC(N)=C1
Synonyms:- 1-Amino-3-nitro-4-methoxybenzene
- 3-Nitro-4-methoxyaniline
- 3-Nitro-p-anisidine
- 4-Amino-2-nitroanisole
- 4-Methoxy-3-nitrobenzenamine
- Benzenamine, 4-methoxy-3-nitro-
- p-Anisidine, 3-nitro-
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Found 5 products.
4-Methoxy-3-Nitroaniline
CAS:Formula:C7H8N2O3Purity:98%Color and Shape:SolidMolecular weight:168.15004-Methoxy-3-nitroaniline
CAS:<p>4-Methoxy-3-nitroaniline</p>Formula:C7H8N2O3Purity:≥95%Color and Shape: red solidMolecular weight:168.15g/mol4-Methoxy-3-nitroaniline
CAS:<p>4-Methoxy-3-nitroaniline is a chemical compound that has been shown to have anti-tumor and anti-inflammatory effects. It belongs to the class of amines and can be synthesized by nitrating 4-methoxy aniline. The reaction product is then reacted with sodium hydroxide in a solution of alcohol and water, which produces 2,4-dinitroaniline. When this substance is heated at high temperatures, it converts into a mixture of products, including 2,4,6-trinitroaniline. This compound has been shown to inhibit tumor growth in rats. Toxicity studies revealed that it was not toxic when administered orally in doses up to 5g/kg body weight for 7 days.</p>Formula:C7H8N2O3Purity:Min. 95%Color and Shape:Orange PowderMolecular weight:168.15 g/mol




