Ethyl 3-methyl-1-phenyl-1H-pyrazole-5-carboxylate, identified by its CAS number 81153-63-1, is an organic compound belonging to the class of pyrazole derivatives. This substance features a pyrazole ring, which is a five-membered ring containing two adjacent nitrogen atoms, contributing to its unique chemical properties. The presence of the ethyl ester group enhances its solubility in organic solvents, making it useful in various chemical reactions and applications. The methyl and phenyl substituents on the pyrazole ring can influence its reactivity and biological activity, potentially making it a candidate for pharmaceutical development. Generally, compounds like this may exhibit a range of biological activities, including anti-inflammatory or analgesic properties, although specific biological data would depend on empirical studies. Additionally, its synthesis typically involves multi-step organic reactions, which may include condensation and esterification processes. As with many organic compounds, proper handling and safety measures should be observed due to potential toxicity or reactivity.

ethyl 3-methyl-1-phenyl-1H-pyrazole-5-carboxylate

81153-63-1: Ethyl 3-methyl-1-phenyl-1H-pyrazole-5-carboxylate, identified by its CAS number 81153-63-1, is an organic compound belonging to the class of pyrazole derivatives. This substance features a pyrazole ring, which is a five-membered ring containing two adjacent nitrogen atoms, contributing to its unique chemical properties. The presence of the ethyl ester group enhances its solubility in organic solvents, making it useful in various chemical reactions and applications. The methyl and phenyl substituents on the pyrazole ring can influence its reactivity and biological activity, potentially making it a candidate for pharmaceutical development. Generally, compounds like this may exhibit a range of biological activities, including anti-inflammatory or analgesic properties, although specific biological data would depend on empirical studies. Additionally, its synthesis typically involves multi-step organic reactions, which may include condensation and esterification processes. As with many organic compounds, proper handling and safety measures should be observed due to potential toxicity or reactivity.

CAS 81153-63-1

ethyl 3-methyl-1-phenyl-1H-pyrazole-5-carboxylate

Ethyl 3-methyl-1-phenyl-1H-pyrazole-5-carboxylate

Ref: IN-DA004ZQF

Ethyl 3-methyl-1-phenyl-1H-pyrazole-5-carboxylate

Ref: 54-OR2705

Ethyl 3-methyl-1-phenylpyrazole-5-carboxylate

Ref: 10-F034022