1-[2,6-Dichloro-4-(fluoromethyl)phenyl]-3-(2-methylpropyl)-1H-pyrazole-5-carboxylic acid ethyl ester, with CAS number 126100-06-9, is a synthetic organic compound characterized by its complex molecular structure. It features a pyrazole ring, which is a five-membered heterocyclic compound containing two nitrogen atoms, contributing to its potential biological activity. The presence of dichloro and fluoromethyl substituents on the phenyl group enhances its lipophilicity and may influence its interaction with biological targets. The ethyl ester functional group suggests that it may undergo hydrolysis to release the corresponding carboxylic acid, which can be relevant in pharmacokinetics. This compound is likely to exhibit specific reactivity due to the electron-withdrawing nature of the halogen substituents, which can affect its acidity and overall stability. Its unique structure may confer specific properties that could be explored in various applications, including agrochemicals or pharmaceuticals, although detailed studies would be necessary to elucidate its full potential and behavior in biological systems.

1-[2,6-DICHLORO-4-(FLUOROMETHYL)PHENYL]-3-(2-METHYLPROPYL)-1H-PYRAZOLE-5-CARBOXYLIC ACID ETHYL ESTER

126100-06-9: 1-[2,6-Dichloro-4-(fluoromethyl)phenyl]-3-(2-methylpropyl)-1H-pyrazole-5-carboxylic acid ethyl ester, with CAS number 126100-06-9, is a synthetic organic compound characterized by its complex molecular structure. It features a pyrazole ring, which is a five-membered heterocyclic compound containing two nitrogen atoms, contributing to its potential biological activity. The presence of dichloro and fluoromethyl substituents on the phenyl group enhances its lipophilicity and may influence its interaction with biological targets. The ethyl ester functional group suggests that it may undergo hydrolysis to release the corresponding carboxylic acid, which can be relevant in pharmacokinetics. This compound is likely to exhibit specific reactivity due to the electron-withdrawing nature of the halogen substituents, which can affect its acidity and overall stability. Its unique structure may confer specific properties that could be explored in various applications, including agrochemicals or pharmaceuticals, although detailed studies would be necessary to elucidate its full potential and behavior in biological systems.

CAS 126100-06-9

1-[2,6-DICHLORO-4-(FLUOROMETHYL)PHENYL]-3-(2-METHYLPROPYL)-1H-PYRAZOLE-5-CARBOXYLIC ACID ETHYL ESTER

1H-Pyrazole-5-carboxylic acid, 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-3-(2-methylpropyl)-, ethyl ester

Ref: IN-DA000RMU