3-bromo-2,4-dimethylaniline

3-bromo-2,4-dimethylaniline

3,5-dimethyl-4-fluorobenzyl bromide

3,5-dimethyl-4-fluorobenzyl bromide

3-amino-2-nitrobenzonitrile

$150.00
CAS No.: 408502-45-4
Catalog No.: WLZ1692
Purity: 95%
MF: C7H5N3O2
MW: 163.136
Storage: 2-8 degree Celsius
SMILES: NC=1C(=C(C#N)C=CC1)[N+](=O)[O-]
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CAS NO.: 408502-45-4; 3-amino-2-nitrobenzonitrile. PROPERTIES: This aromatic compound features an amine group, a nitro group, and a nitrile group on a benzene ring, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 3-amino-2-nitrobenzonitrile typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes electron-withdrawing nitro and nitrile groups and an electron-donating amine group that influence the electronic properties of the aromatic system. For optimal stability and to prevent degradation, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, appropriate safety measures including nitrile gloves and safety goggles are essential. This compound is sensitive to moisture and may hydrolyze in aqueous environments. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 3-amino-2-nitrobenzonitrile serves as a valuable intermediate in the synthesis of highly functionalized aromatic compounds and materials with specific electronic properties. The nitro group provides a handle for further functionalization through reduction to amine or other transformations. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The nitrile and amine substituents contribute to target binding affinity and selectivity. Additionally, the molecule finds utility in materials science as a monomer for creating polymers with specific electronic and optical properties. Researchers utilizing this compound benefit from its functional group versatility, enabling the development of diverse molecular architectures for applications ranging from drug discovery to advanced materials.

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