Product Name:2-fluoro-4-methyl-6-nitrophenol

IUPAC Name:2-fluoro-4-methyl-6-nitrophenol

CAS:2070-43-1
Molecular Formula:C7H6FNO3
Purity:95%
Catalog Number:CM128064
Molecular Weight:171.13

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For R&D use only.

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Product Details

CAS NO:2070-43-1
Molecular Formula:C7H6FNO3
Melting Point:-
Smiles Code:OC1=C([N+]([O-])=O)C=C(C)C=C1F
Density:
Catalog Number:CM128064
Molecular Weight:171.13
Boiling Point:
MDL No:MFCD16658596
Storage:Store at 2-8°C.

Category Infos

Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

Product Other Information

Product Overview 2-fluoro-4-methyl-6-nitrophenol, also known as FMN, is a synthetic compound with a wide range of applications in the field of chemistry. It is a phenol with a nitro group attached to the 6-position on the aromatic ring, and a fluorine atom attached to the 2-position. It is an important intermediate for the synthesis of many pharmaceuticals, as well as for the production of dyes and other industrial chemicals. In addition to its use in industrial applications, FMN has recently been studied for its potential use in scientific research and medical applications.
Synthesis and Application 2-fluoro-4-methyl-6-nitrophenol can be synthesized using a number of methods, including the nitration of 2-fluoro-4-methylphenol, the reaction of 4-methyl-6-nitrophenol with fluorine, and the reaction of 2-fluoro-4-methylphenol with nitric acid. The most common method is the nitration of 2-fluoro-4-methylphenol with a mixture of nitric and sulfuric acids. This method produces a high yield of 2-fluoro-4-methyl-6-nitrophenol, usually greater than 95%. 2-fluoro-4-methyl-6-nitrophenol has recently been studied for its potential use in scientific research as a probe for certain types of enzymes. It is a potent inhibitor of the enzyme xanthine oxidase, and has been used to study the enzyme's activity in various biological systems. 2-fluoro-4-methyl-6-nitrophenol has also been used to study the activity of other enzymes, such as cytochrome P450.
Future Directions There are several potential future directions for the use of 2-fluoro-4-methyl-6-nitrophenol. It could be used as a probe for the study of other enzymes, or as an inhibitor of certain enzymes. It could also be used in the development of new drugs, or as a potential treatment for certain diseases. In addition, it could be used to study the biochemistry and physiology of certain organisms, or as a potential source of new dyes and other industrial chemicals.