Phenol, 2-fluoro-3-nitro- (CAS 179816-26-3) is an aromatic compound characterized by the presence of a hydroxyl group (-OH) attached to a benzene ring, which is further substituted with a fluorine atom at the ortho position and a nitro group (-NO2) at the meta position relative to the hydroxyl group. This compound exhibits typical phenolic properties, including moderate solubility in water due to the polar hydroxyl group, while the presence of the nitro and fluoro substituents can influence its reactivity and polarity. The nitro group is an electron-withdrawing group, which can enhance the acidity of the hydroxyl group, making it more likely to participate in electrophilic substitution reactions. Additionally, the fluorine atom can impart unique electronic and steric effects, potentially affecting the compound's biological activity and interactions with other molecules. Overall, 2-fluoro-3-nitrophenol is of interest in various fields, including pharmaceuticals and materials science, due to its potential applications and reactivity.

Phenol, 2-fluoro-3-nitro-

179816-26-3: 2-Fluoro-3-nitrophenol,  phenol, 2-fluoro-3-nitro-

2-Fluoro-3-nitrophenol is a phenolic compound that is found in the environment. It has been shown to have an electrophilic nature and can react with other cellular components, such as proteins and DNA. 2-Fluoro-3-nitrophenol has been shown to be cytotoxic to rat liver microsomes. This property may be due to its ability to form reactive metabolites, such as fluorine and bromine, which are capable of reacting with macromolecules in the cell. 2-Fluoro-3-nitrophenol has also been shown to bind covalently with albumin and serum albumin, which may account for its toxicity.

CAS 179816-26-3: Phenol, 2-fluoro-3-nitro-

2-fluoro-3-nitrophenol

Ref: 3D-FF104666

2-Fluoro-3-nitrophenol

Ref: 54-PC53465

2-Fluoro-3-nitrophenol

Ref: 10-F077045

Phenol, 2-fluoro-3-nitro-

Ref: IN-DA0027AB