1-(4-Fluorophenyl)-1H-pyrrole-2,5-dione, with the CAS number 6633-22-3, is a chemical compound characterized by its unique structure, which includes a pyrrole ring substituted with a fluorophenyl group. This compound typically exhibits a yellow to orange color and is known for its potential applications in organic synthesis and medicinal chemistry. The presence of the fluorine atom enhances its electronic properties, potentially influencing its reactivity and biological activity. As a diketone, it can participate in various chemical reactions, including nucleophilic additions and cycloadditions. The compound's solubility may vary depending on the solvent, and it is generally stable under standard conditions. However, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Its specific properties, such as melting point, boiling point, and spectral characteristics, can be determined through experimental methods and are essential for its application in research and industry.

1-(4-Fluorophenyl)-1H-pyrrole-2,5-dione

6633-22-3: 1H-Pyrrole-2,5-dione, 1-(4-fluorophenyl)-

N-(4-Fluoro-phenyl)maleimide

1-(4-Fluoro-Phenyl)-Pyrrole-2,5-Dione is a chemical compound that has two isomers. The more stable of the two isomers is the trans form, which can be polymerized and undergoes photochromism (becoming colorless in sunlight). The less stable cis form of 1-(4-Fluoro-Phenyl)-Pyrrole-2,5-Dione exists in equilibrium with the trans form at reaction temperatures. It also reacts with chloride to give aziridines. This compound can be prepared by a stepwise process involving nucleophilic substitution and elimination reactions at temperatures below 100°C.

CAS 6633-22-3: 1-(4-Fluorophenyl)-1H-pyrrole-2,5-dione

N-(4-Fluoro-phenyl)maleimide

Ref: 54-PC11121

1-(4-Fluoro-Phenyl)-Pyrrole-2,5-Dione

Ref: 3D-FF83421

N-(4-Fluorophenyl)maleimide

Ref: 3B-F1054

1-(4-FLUORO-PHENYL)-PYRROLE-2,5-DIONE

Ref: IN-DA00FAOL

1-(4-Fluorophenyl)-pyrrole-2,5-dione

Ref: 10-F015222