Ethyl 5-amino-1-(pyridin-2-yl)-1H-pyrazole-4-carboxylate, with the CAS number 69722-29-8, is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two adjacent nitrogen atoms. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of an amino group and a pyridine ring enhances its potential for biological activity, making it of interest in medicinal chemistry. Typically, compounds like this may exhibit properties such as moderate to high polarity due to the presence of functional groups, which can influence their interaction with biological systems. Additionally, the structural features suggest potential applications in drug development, particularly in targeting specific enzymes or receptors. Its synthesis and characterization would involve standard organic chemistry techniques, and it may be studied for its pharmacological properties, including anti-inflammatory or antimicrobial activities. As with many organic compounds, safety data sheets should be consulted for handling and storage guidelines.

ethyl 5-amino-1-(pyridin-2-yl)-1H-pyrazole-4-carboxylate

69722-29-8: Ethyl 5-amino-1-(pyridin-2-yl)-1H-pyrazole-4-carboxylate, with the CAS number 69722-29-8, is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two adjacent nitrogen atoms. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of an amino group and a pyridine ring enhances its potential for biological activity, making it of interest in medicinal chemistry. Typically, compounds like this may exhibit properties such as moderate to high polarity due to the presence of functional groups, which can influence their interaction with biological systems. Additionally, the structural features suggest potential applications in drug development, particularly in targeting specific enzymes or receptors. Its synthesis and characterization would involve standard organic chemistry techniques, and it may be studied for its pharmacological properties, including anti-inflammatory or antimicrobial activities. As with many organic compounds, safety data sheets should be consulted for handling and storage guidelines.

CAS 69722-29-8

ethyl 5-amino-1-(pyridin-2-yl)-1H-pyrazole-4-carboxylate

5-Amino-1-(2-pyridinyl)-1H-pyrazole-4-carboxylic acid, ethyl ester

Ref: 54-OR302036

Ethyl 5-amino-1-(pyridin-2-yl)-1H-pyrazole-4-carboxylate

Ref: 10-F336135