Ethyl 1-(4-fluorophenyl)-5-iodo-1H-pyrazole-4-carboxylate is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. The presence of a 4-fluorophenyl group indicates that a fluorine atom is substituted on a phenyl ring at the para position, contributing to the compound's potential biological activity and lipophilicity. The iodo substituent at the 5-position of the pyrazole ring enhances its reactivity and may influence its pharmacological properties. The ethyl ester functional group at the carboxylate position suggests that this compound may be involved in esterification reactions or serve as a prodrug. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, as pyrazole derivatives often exhibit a range of biological activities, including anti-inflammatory and anticancer properties. Its molecular structure and substituents can significantly affect its solubility, stability, and interaction with biological targets.

ETHYL 1-(4-FLUOROPHENYL)-5-IODO-1H-PYRAZOLE-4-CARBOXYLATE

959576-71-7: Ethyl 1-(4-fluorophenyl)-5-iodo-1H-pyrazole-4-carboxylate is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. The presence of a 4-fluorophenyl group indicates that a fluorine atom is substituted on a phenyl ring at the para position, contributing to the compound's potential biological activity and lipophilicity. The iodo substituent at the 5-position of the pyrazole ring enhances its reactivity and may influence its pharmacological properties. The ethyl ester functional group at the carboxylate position suggests that this compound may be involved in esterification reactions or serve as a prodrug. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, as pyrazole derivatives often exhibit a range of biological activities, including anti-inflammatory and anticancer properties. Its molecular structure and substituents can significantly affect its solubility, stability, and interaction with biological targets.

<p>Ethyl 1-(4-fluorophenyl)-5-iodo-1H-pyrazole-4-carboxylate</p>

CAS 959576-71-7

ETHYL 1-(4-FLUOROPHENYL)-5-IODO-1H-PYRAZOLE-4-CARBOXYLATE

Ethyl 1-(4-fluorophenyl)-5-iodo-1H-pyrazole-4-carboxylate

Ref: 54-PC10246