2,6-dichloro-4-fluorobenzonitrile
$300.00
CAS No.: 1473423-59-4
Catalog No.: 193879
Purity: 95%
MF: C7H2Cl2FN
MW: 190.004
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C#N)C(=CC(=C1)F)Cl
Catalog No.: 193879
Purity: 95%
MF: C7H2Cl2FN
MW: 190.004
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C#N)C(=CC(=C1)F)Cl
2,6-dichloro-4-fluorobenzonitrile; CAS No.: 1473423-59-4;2,6-dichloro-4-fluorobenzonitrile. PROPERTIES: 2,6-dichloro-4-fluorobenzonitrile is a chlorinated and fluorinated aromatic nitrile with molecular formula C7H3Cl2FNO. It typically exists as a colorless liquid with a boiling point around 135-140 C. The compound has limited water solubility but dissolves well in organic solvents like dichloromethane or THF. It exhibits moderate thermal stability but may decompose when exposed to high temperatures or strong bases, releasing toxic chlorine and fluorine-containing fumes. Proper storage involves keeping it in tightly sealed containers below 25 C, away from heat sources and incompatible materials. APPLICATIONS: In organic synthesis, this compound serves as a valuable intermediate for developing agrochemicals. The dichloro and fluoro substitution provides electron-withdrawing effects that enhance herbicidal activity, while the nitrile group offers sites for further functionalization (Pest Management Science). In materials science, 2,6-dichloro-4-fluorobenzonitrile contributes to the creation of functional organic materials with tailored electronic properties. Its fluorinated aromatic core and nitrile group influence the electronic characteristics of derived materials, useful in optoelectronic applications such as organic light-emitting diodes (Chemistry of Materials). The nitrile group can be further transformed through hydrolysis or reduction to form amides or amines, expanding its utility in multistep syntheses (The Journal of Organic Chemistry).
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