1-(4-Fluorophenyl)-5-phenyl-pyrazole, identified by its CAS number 299162-83-7, is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features a 4-fluorophenyl group and a phenyl group attached to the pyrazole structure, contributing to its unique chemical properties. The presence of the fluorine atom enhances its lipophilicity and may influence its biological activity, making it of interest in medicinal chemistry. The compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds with anti-inflammatory or analgesic properties. Additionally, the presence of aromatic rings may contribute to its stability and reactivity, making it a candidate for further research in various chemical and biological contexts. As with many pyrazole derivatives, it may also be explored for its potential in agrochemical applications.

1-(4-fluorophenyl)-5-phenyl-pyrazole

299162-83-7: 1-(4-Fluorophenyl)-5-phenyl-pyrazole, identified by its CAS number 299162-83-7, is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features a 4-fluorophenyl group and a phenyl group attached to the pyrazole structure, contributing to its unique chemical properties. The presence of the fluorine atom enhances its lipophilicity and may influence its biological activity, making it of interest in medicinal chemistry. The compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds with anti-inflammatory or analgesic properties. Additionally, the presence of aromatic rings may contribute to its stability and reactivity, making it a candidate for further research in various chemical and biological contexts. As with many pyrazole derivatives, it may also be explored for its potential in agrochemical applications.

CAS 299162-83-7

1-(4-fluorophenyl)-5-phenyl-pyrazole

1-(4-FLUOROPHENYL)-5-PHENYL-1H-PYRAZOLE

Ref: IN-DA00C4EV

1-(4-Fluorophenyl)-5-phenyl-1H-pyrazole

Ref: 10-F336231