5-(3-Chlorophenyl)-1H-pyrazole is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. The presence of a 3-chlorophenyl group at the 5-position of the pyrazole ring contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic aromatic structure. It is often studied for its potential biological activities, including anti-inflammatory and analgesic properties, making it of interest in medicinal chemistry. The chlorophenyl substituent can influence the compound's reactivity and interaction with biological targets. Additionally, the compound's molecular structure allows for various synthetic modifications, which can lead to derivatives with enhanced or altered properties. As with many pyrazole derivatives, it may also exhibit interesting electronic characteristics due to the presence of the nitrogen atoms in the ring, which can affect its behavior in chemical reactions and interactions with other molecules.

5-(3-chlorophenyl)-1H-pyrazole

59843-69-5: 5-(3-Chlorophenyl)-1H-pyrazole is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. The presence of a 3-chlorophenyl group at the 5-position of the pyrazole ring contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic aromatic structure. It is often studied for its potential biological activities, including anti-inflammatory and analgesic properties, making it of interest in medicinal chemistry. The chlorophenyl substituent can influence the compound's reactivity and interaction with biological targets. Additionally, the compound's molecular structure allows for various synthetic modifications, which can lead to derivatives with enhanced or altered properties. As with many pyrazole derivatives, it may also exhibit interesting electronic characteristics due to the presence of the nitrogen atoms in the ring, which can affect its behavior in chemical reactions and interactions with other molecules.

CAS 59843-69-5

5-(3-chlorophenyl)-1H-pyrazole

5-(3-Chlorophenyl)-1H-pyrazole

Ref: IN-DA003I28

3-(3-Chlorophenyl)-1H-pyrazole

Ref: 54-OR17

5-(3-CHLOROPHENYL)-1H-PYRAZOLE

Ref: 10-F300908