2-chloro-4-(trifluoromethoxy)nitrobenzene
$365.00
CAS No.: 85578-47-8
Catalog No.: 193922
Purity: 95%
MF: C7H3ClF3NO3
MW: 241.552
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C=CC(=C1)OC(F)(F)F)[N+](=O)[O-]
Catalog No.: 193922
Purity: 95%
MF: C7H3ClF3NO3
MW: 241.552
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C=CC(=C1)OC(F)(F)F)[N+](=O)[O-]
2-chloro-4-(trifluoromethoxy)nitrobenzene; CAS No.: 85578-47-8;2-chloro-4-(trifluoromethoxy)nitrobenzene. PROPERTIES: 2-chloro-4-(trifluoromethoxy)nitrobenzene is a chlorinated and trifluoromethylated aromatic nitro compound with molecular formula C7H3ClF3NO3. It typically exists as a colorless liquid with a boiling point around 130-135 C. The compound has limited water solubility but dissolves well in organic solvents like chloroform or carbon tetrachloride. It exhibits moderate thermal stability but may decompose when exposed to high temperatures or strong bases, releasing toxic nitrogen oxides and chlorine-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 chloro and trifluoromethoxy substitution provides electron-withdrawing effects that enhance herbicidal activity, while the nitro group offers sites for further functionalization (Pest Management Science). In materials science, 2-chloro-4-(trifluoromethoxy)nitrobenzene contributes to the creation of functional organic materials with tailored electronic properties. Its fluorinated aromatic core and nitro group influence the electronic characteristics of derived materials, useful in optoelectronic applications such as organic light-emitting diodes (Chemistry of Materials). The nitro group can be further transformed through reduction to form amines, expanding its utility in multistep syntheses (The Journal of Organic Chemistry).
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