2,4-Difluoronitrobenzene has been used in the synthesis of 2,4-difluoro-5-nitrobenzenesulfonic acid via sulfonation reaction, (±)-horsfiline and resin-bound-2-arylaminobenzimidazoles.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2,4-Difluoronitrobenzene has been used in the synthesis of 2,4-difluoro-5-nitrobenzenesulfonic acid via sulfonation reaction, (±)-horsfiline and resin-bound-2-arylaminobenzimidazoles.
Solubility
Insoluble in water.
Notes
Store at room temperature. Incompatible with oxidizing agents. Ensure adequate ventilation.
RUO – Research Use Only
General References:
- W. Cameron Black .; Benoit Guay.; Frank Scheuermeyer. Metalation of Nitroaromatics with in Situ Electrophiles. J. Org. Chem. 1997, 62 (3), 758-760 .
- Guanyu Yang.; Qiaohong Zhang .; Hong Miao.; Xinli Tong.; Jie Xu. Selective Organocatalytic Oxygenation of Hydrocarbons by Dioxygen Using Anthraquinones and N-Hydroxyphthalimide.Org. Lett. 2005, 7 (2),263-266 .
- Nucleophilic displacement of the activated fluorines with 2-ethyl-4-methylimidazole occurs predominantly at the 2-position, or, under more forcing conditions, at both 2- and 4-positions: J. Med. Chem., 34, 2671 (1991).