(E)-3-(4-Fluorobenzylidene)-2,3-dihydrochromen-4-one is an organic compound characterized by its chromenone structure, which features a fused benzene and pyrone ring. The presence of a 4-fluorobenzylidene substituent indicates that it has a fluorine atom attached to a benzyl group, contributing to its electronic properties and potentially influencing its reactivity and biological activity. This compound typically exhibits a yellow to orange color due to its conjugated system, which allows for light absorption in the visible spectrum. It may possess interesting pharmacological properties, making it a subject of research in medicinal chemistry. The compound's structure suggests it could participate in various chemical reactions, including nucleophilic attacks and electrophilic substitutions, due to the presence of reactive sites. Additionally, its solubility and stability can vary depending on the solvent and environmental conditions. Overall, (E)-3-(4-Fluorobenzylidene)-2,3-dihydrochromen-4-one is notable for its unique structural features and potential applications in drug development and organic synthesis.

(E)-3-(4-FLUOROBENZYLIDENE)-2,3-DIHYDROCHROMEN-4-ONE

948307-89-9: (E)-3-(4-Fluorobenzylidene)-2,3-dihydrochromen-4-one is an organic compound characterized by its chromenone structure, which features a fused benzene and pyrone ring. The presence of a 4-fluorobenzylidene substituent indicates that it has a fluorine atom attached to a benzyl group, contributing to its electronic properties and potentially influencing its reactivity and biological activity. This compound typically exhibits a yellow to orange color due to its conjugated system, which allows for light absorption in the visible spectrum. It may possess interesting pharmacological properties, making it a subject of research in medicinal chemistry. The compound's structure suggests it could participate in various chemical reactions, including nucleophilic attacks and electrophilic substitutions, due to the presence of reactive sites. Additionally, its solubility and stability can vary depending on the solvent and environmental conditions. Overall, (E)-3-(4-Fluorobenzylidene)-2,3-dihydrochromen-4-one is notable for its unique structural features and potential applications in drug development and organic synthesis.

CAS 948307-89-9

(E)-3-(4-FLUOROBENZYLIDENE)-2,3-DIHYDROCHROMEN-4-ONE