Ethyl 5-chloro-1-phenyl-1H-pyrazole-4-carboxylate is a chemical compound characterized by its pyrazole ring structure, which is a five-membered ring containing two adjacent nitrogen atoms. This compound features a chloro substituent at the 5-position and a phenyl group at the 1-position of the pyrazole ring, contributing to its aromatic properties. The ethyl ester functional group at the 4-position enhances its solubility in organic solvents and may influence its reactivity. Typically, compounds of this nature exhibit biological activity, making them of interest in medicinal chemistry and agrochemical applications. The presence of the chloro group can also affect the compound's electronic properties and reactivity, potentially enhancing its interaction with biological targets. Ethyl 5-chloro-1-phenyl-1H-pyrazole-4-carboxylate is likely to be a solid at room temperature, with potential applications in pharmaceuticals or as an intermediate in organic synthesis. As with many pyrazole derivatives, it may exhibit a range of biological activities, warranting further investigation into its pharmacological properties.

ethyl 5-chloro-1-phenyl-1H-pyrazole-4-carboxylate

98534-76-0: Ethyl 5-chloro-1-phenyl-1H-pyrazole-4-carboxylate is a chemical compound characterized by its pyrazole ring structure, which is a five-membered ring containing two adjacent nitrogen atoms. This compound features a chloro substituent at the 5-position and a phenyl group at the 1-position of the pyrazole ring, contributing to its aromatic properties. The ethyl ester functional group at the 4-position enhances its solubility in organic solvents and may influence its reactivity. Typically, compounds of this nature exhibit biological activity, making them of interest in medicinal chemistry and agrochemical applications. The presence of the chloro group can also affect the compound's electronic properties and reactivity, potentially enhancing its interaction with biological targets. Ethyl 5-chloro-1-phenyl-1H-pyrazole-4-carboxylate is likely to be a solid at room temperature, with potential applications in pharmaceuticals or as an intermediate in organic synthesis. As with many pyrazole derivatives, it may exhibit a range of biological activities, warranting further investigation into its pharmacological properties.

CAS 98534-76-0

ethyl 5-chloro-1-phenyl-1H-pyrazole-4-carboxylate

Ethyl 5-chloro-1-phenyl-1H-pyrazole-4-carboxylate

Ref: IN-DA00IK4C