2-(Difluoromethoxy)-3-fluoronitrobenzene is an organic compound characterized by the presence of a nitro group, a fluorine atom, and a difluoromethoxy substituent on a benzene ring. This compound features a nitro group (-NO2) that is known for its electron-withdrawing properties, which can influence the reactivity and stability of the molecule. The difluoromethoxy group (-O-CHF2) introduces both electronegative fluorine atoms and an ether functionality, contributing to the compound's overall polarity and potential for hydrogen bonding. The presence of multiple fluorine atoms enhances the compound's lipophilicity and may affect its solubility in various solvents. Additionally, the arrangement of substituents on the benzene ring can lead to unique electronic properties, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. The compound's specific reactivity and interactions would depend on its molecular structure and the environment in which it is used. Safety and handling considerations should be taken into account due to the presence of the nitro group and fluorinated moieties.

2-(difluoromethoxy)-3-fluoronitrobenzene

1214326-22-3: 2-(Difluoromethoxy)-3-fluoronitrobenzene is an organic compound characterized by the presence of a nitro group, a fluorine atom, and a difluoromethoxy substituent on a benzene ring. This compound features a nitro group (-NO2) that is known for its electron-withdrawing properties, which can influence the reactivity and stability of the molecule. The difluoromethoxy group (-O-CHF2) introduces both electronegative fluorine atoms and an ether functionality, contributing to the compound's overall polarity and potential for hydrogen bonding. The presence of multiple fluorine atoms enhances the compound's lipophilicity and may affect its solubility in various solvents. Additionally, the arrangement of substituents on the benzene ring can lead to unique electronic properties, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. The compound's specific reactivity and interactions would depend on its molecular structure and the environment in which it is used. Safety and handling considerations should be taken into account due to the presence of the nitro group and fluorinated moieties.

<p>2-(Difluoromethoxy)-3-fluoronitrobenzene</p>

CAS 1214326-22-3

2-(difluoromethoxy)-3-fluoronitrobenzene

2-(Difluoromethoxy)-3-fluoronitrobenzene

Ref: 54-PC501882