2,6-bis(trifluoromethyl)benzonitrile
$350.00
CAS No.: 25753-25-7
Catalog No.: WLZ1609
Purity: 95%
MF: C9H3F6N
MW: 239.118
Storage: 2-8 degree Celsius
SMILES: FC(C1=C(C#N)C(=CC=C1)C(F)(F)F)(F)F
Catalog No.: WLZ1609
Purity: 95%
MF: C9H3F6N
MW: 239.118
Storage: 2-8 degree Celsius
SMILES: FC(C1=C(C#N)C(=CC=C1)C(F)(F)F)(F)F
CAS NO.: 25753-25-7; 2,6-bis(trifluoromethyl)benzonitrile. PROPERTIES: This fluorinated aromatic compound features two trifluoromethyl groups on a benzene ring connected to a nitrile group, creating a molecule with potential applications in organic synthesis and materials science. The 2,6-bis(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 groups 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 2,6-bis(trifluoromethyl)benzonitrile serves as a valuable intermediate in the synthesis of highly fluorinated compounds and materials with specific electronic properties. The trifluoromethyl groups provide handles for further functionalization through nucleophilic substitution reactions. In materials science, this compound functions as a building block for creating polymers and small molecules with applications in organic electronics and optoelectronics. Additionally, the molecule finds utility in chemical biology studies where its unique electronic properties can be harnessed for developing novel imaging agents and sensors. Researchers utilizing this compound benefit from its defined halogenation pattern, enabling the development of advanced materials with tailored electronic and optical characteristics.
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