2,6-Difluoro-4-nitrophenol is an organic compound characterized by the presence of two fluorine atoms and a nitro group attached to a phenolic ring. Its molecular formula is C6H4F2N2O3, indicating a structure that includes a hydroxyl group (-OH) and a nitro group (-NO2) on the aromatic ring. The fluorine substituents are located at the 2 and 6 positions, while the nitro group is at the 4 position, contributing to the compound's reactivity and potential applications in various chemical processes. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. It is known for its use in the synthesis of other chemical compounds and may serve as an intermediate in the production of agrochemicals or pharmaceuticals. Additionally, due to the presence of both electron-withdrawing groups (fluorine and nitro), it can exhibit unique electronic properties, influencing its behavior in chemical reactions. Safety precautions should be taken when handling this compound, as it may pose health and environmental risks.

2,6-Difluoro-4-nitrophenol

658-07-1: 4-Nitro-2,6-difluorophenol, Phenol, 2,6-Difluoro-4-Nitro-, Wnr Dq Cf Ef [Wln], 2,6-Difluoro-4-nitrophenol , 2,6-Difluoro-4-nitrophenol

2,6-Difluoro-4-nitrophenol is a chemical compound that has been used to detect chlorine atoms in the atmosphere. It is produced by the reaction of nitric acid with acetaminophen and protonated with hydroxyl ions. The nitro group then reacts with a hydroxyl group to form 2,6-difluoro-4-hydroxynitrophenol. A fluorine atom can be substituted at the terminal position of the benzene ring. This compound has been synthesized and characterized using x-ray crystal structures of its dehydrogenase enzymes.

CAS 658-07-1: 2,6-Difluoro-4-nitrophenol

2,6-Difluoro-4-nitrophenol

Ref: 10-F076162

2,6-Difluoro-4-nitrophenol

Ref: 54-PC9845

2,6-difluoro-4-nitrophenol

Ref: 3D-FD104934

2,6-Difluoro-4-nitrophenol

Ref: IN-DA00FD6N