Ethyl-3-(2-chlorophenyl)-pyrazole-4-carboxylate, with the CAS number 149740-12-5, is a chemical compound that belongs to the class of pyrazole derivatives. It features a pyrazole ring, which is a five-membered ring containing two nitrogen atoms, and is substituted with an ethyl ester and a 2-chlorophenyl group. This compound is characterized by its potential biological activity, often explored in medicinal chemistry for its applications in pharmaceuticals. The presence of the chlorophenyl moiety may influence its lipophilicity and biological interactions, making it a subject of interest in drug development. Ethyl-3-(2-chlorophenyl)-pyrazole-4-carboxylate may exhibit various properties such as solubility in organic solvents, stability under specific conditions, and reactivity with other chemical agents. Its synthesis typically involves multi-step organic reactions, and it may be analyzed using techniques like NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, this compound represents a significant area of research in the field of organic and medicinal chemistry.

ETHYL-3-(2-CHLOROPHENYL)-PYRAZOLE-4-CARBOXYLATE

149740-12-5: Ethyl-3-(2-chlorophenyl)-pyrazole-4-carboxylate, with the CAS number 149740-12-5, is a chemical compound that belongs to the class of pyrazole derivatives. It features a pyrazole ring, which is a five-membered ring containing two nitrogen atoms, and is substituted with an ethyl ester and a 2-chlorophenyl group. This compound is characterized by its potential biological activity, often explored in medicinal chemistry for its applications in pharmaceuticals. The presence of the chlorophenyl moiety may influence its lipophilicity and biological interactions, making it a subject of interest in drug development. Ethyl-3-(2-chlorophenyl)-pyrazole-4-carboxylate may exhibit various properties such as solubility in organic solvents, stability under specific conditions, and reactivity with other chemical agents. Its synthesis typically involves multi-step organic reactions, and it may be analyzed using techniques like NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, this compound represents a significant area of research in the field of organic and medicinal chemistry.

CAS 149740-12-5

ETHYL-3-(2-CHLOROPHENYL)-PYRAZOLE-4-CARBOXYLATE

1H-Pyrazole-4-carboxylic acid, 3-(2-chlorophenyl)-, ethyl ester

Ref: IN-DA001M04

ethyl 5-(2-chlorophenyl)-1H-pyrazole-4-carboxylate

Ref: 10-F525888