2-Chloro-1-fluoro-4-methoxybenzene, also known by its CAS number 202925-07-3, is an aromatic compound characterized by the presence of a methoxy group (-OCH3), a chlorine atom, and a fluorine atom attached to a benzene ring. This compound features a substituted benzene structure, which contributes to its chemical reactivity and physical properties. It typically exhibits a moderate boiling point and melting point, indicative of its molecular weight and the presence of polar functional groups. The methoxy group can influence the compound's solubility in organic solvents, often making it more soluble due to its electron-donating properties. The chlorine and fluorine substituents can enhance the compound's reactivity, making it useful in various chemical syntheses and applications, including pharmaceuticals and agrochemicals. Additionally, the presence of halogens can impart unique electronic properties, affecting the compound's behavior in chemical reactions. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

2-Chloro-1-fluoro-4-methoxybenzene

202925-07-3: 2-Chloro-1-Fluoro-4-Methoxybenzene, Benzene, 2-chloro-1-fluoro-4-methoxy-, 3-Chloro-4-fluoroanisole

3-Chloro-4-fluoroanisole

3-Chloro-4-fluoroanisole is a chlorinated aromatic compound that has been shown to have vibrational and isotopic effects. It can be used as a diphosphine ligand in catalytic reactions involving transition metal complexes. 3-Chloro-4-fluoroanisole has an ionization energy of 60 kcal/mol, which is the energy needed to remove an electron from the covalent bond with fluorine. This chemical also has conformational and functional properties, which stem from its substituent effects on the molecule.

CAS 202925-07-3: 2-Chloro-1-fluoro-4-methoxybenzene

3-Chloro-4-fluoroanisole

Ref: 10-F013257

3-Chloro-4-fluoroanisole

Ref: 3D-FC96013

Benzene, 2-chloro-1-fluoro-4-methoxy-

Ref: IN-DA0028KN

3-Chloro-4-fluoroanisole

Ref: 3B-C2217

3-Chloro-4-fluoroanisole

Ref: 54-PC4082