4-Chloro-1-ethyl-1H-pyrazole-3-carboxylic acid is a heterocyclic organic compound characterized by the presence of a pyrazole ring, which is a five-membered ring containing two nitrogen atoms. The compound features a chloro substituent at the 4-position and an ethyl group at the 1-position of the pyrazole ring, along with a carboxylic acid functional group at the 3-position. This structure imparts unique chemical properties, including potential acidity due to the carboxylic acid group, which can participate in proton transfer reactions. The presence of the chloro group may enhance the compound's reactivity and influence its biological activity. Additionally, the ethyl group contributes to the compound's hydrophobic characteristics, which can affect its solubility in various solvents. This compound may be of interest in pharmaceutical research and agrochemical applications due to its potential biological activities, including herbicidal or fungicidal properties. As with many pyrazole derivatives, it may also exhibit interesting interactions with biological targets, making it a subject of study in medicinal chemistry.

4-chloro-1-ethyl-1H-pyrazole-3-carboxylic acid

512810-20-7: 4-Chloro-1-ethyl-1H-pyrazole-3-carboxylic acid is a heterocyclic organic compound characterized by the presence of a pyrazole ring, which is a five-membered ring containing two nitrogen atoms. The compound features a chloro substituent at the 4-position and an ethyl group at the 1-position of the pyrazole ring, along with a carboxylic acid functional group at the 3-position. This structure imparts unique chemical properties, including potential acidity due to the carboxylic acid group, which can participate in proton transfer reactions. The presence of the chloro group may enhance the compound's reactivity and influence its biological activity. Additionally, the ethyl group contributes to the compound's hydrophobic characteristics, which can affect its solubility in various solvents. This compound may be of interest in pharmaceutical research and agrochemical applications due to its potential biological activities, including herbicidal or fungicidal properties. As with many pyrazole derivatives, it may also exhibit interesting interactions with biological targets, making it a subject of study in medicinal chemistry.

CAS 512810-20-7

4-chloro-1-ethyl-1H-pyrazole-3-carboxylic acid

4-Chloro-1-ethyl-1H-pyrazole-3-carboxylic acid

Ref: 10-F014546