2-amino-6-(trifluoromethyl)benzonitrile
$200.00
CAS No.: 58458-11-0
Catalog No.: WLZ1621
Purity: 95%
MF: C8H5F3N2
MW: 186.136
Storage: 2-8 degree Celsius
SMILES: NC1=C(C#N)C(=CC=C1)C(F)(F)F
Catalog No.: WLZ1621
Purity: 95%
MF: C8H5F3N2
MW: 186.136
Storage: 2-8 degree Celsius
SMILES: NC1=C(C#N)C(=CC=C1)C(F)(F)F
CAS NO.: 58458-11-0; 2-amino-6-(trifluoromethyl)benzonitrile. PROPERTIES: This fluorinated aromatic compound features an amine group and a trifluoromethyl group on a benzene ring connected to a nitrile group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 2-amino-6-(trifluoromethyl)benzonitrile typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes electron-withdrawing trifluoromethyl group and an amine functionality 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 2-amino-6-(trifluoromethyl)benzonitrile serves as a valuable intermediate in the synthesis of fluorinated compounds and materials with specific electronic properties. The trifluoromethyl group provides handles for further functionalization through nucleophilic substitution reactions. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The amine group can be further modified for additional diversification. 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 defined halogenation pattern and functional group arrangement, enabling the development of advanced materials with tailored electronic characteristics.
Reviews
Write Your Own Review