5-Amino-1-[5-(fluoromethyl)phenyl]-1H-pyrazole-4-carboxylic acid ethyl ester, with the CAS number 110821-29-9, is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features an amino group and a carboxylic acid ester functionality, contributing to its potential as a bioactive molecule. The presence of a fluoromethyl group on the phenyl ring enhances its lipophilicity and may influence its biological activity. The ethyl ester moiety can affect the solubility and permeability of the compound, making it relevant in medicinal chemistry. Typically, such compounds are investigated for their pharmacological properties, including anti-inflammatory or analgesic effects. The structural features suggest that it may interact with specific biological targets, making it of interest in drug development. As with many pyrazole derivatives, the compound's reactivity and stability can be influenced by the substituents on the ring, which may also play a role in its synthesis and application in various chemical contexts.

5-AMINO-1-[5-(FLUOROMETHYL)PHENYL]-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER

110821-29-9: 5-Amino-1-[5-(fluoromethyl)phenyl]-1H-pyrazole-4-carboxylic acid ethyl ester, with the CAS number 110821-29-9, is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features an amino group and a carboxylic acid ester functionality, contributing to its potential as a bioactive molecule. The presence of a fluoromethyl group on the phenyl ring enhances its lipophilicity and may influence its biological activity. The ethyl ester moiety can affect the solubility and permeability of the compound, making it relevant in medicinal chemistry. Typically, such compounds are investigated for their pharmacological properties, including anti-inflammatory or analgesic effects. The structural features suggest that it may interact with specific biological targets, making it of interest in drug development. As with many pyrazole derivatives, the compound's reactivity and stability can be influenced by the substituents on the ring, which may also play a role in its synthesis and application in various chemical contexts.

CAS 110821-29-9

5-AMINO-1-[5-(FLUOROMETHYL)PHENYL]-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER

Ethyl 5-amino-1-(3-(fluoromethyl)phenyl)-1H-pyrazole-4-carboxylate

Ref: IN-DA007C2T