5-Amino-1-(4-bromophenyl)-1H-pyrazole-4-carboxylic acid is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), contributing to its potential as a biologically active molecule. The presence of the 4-bromophenyl substituent enhances its lipophilicity and may influence its interaction with biological targets. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid functionality. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as pyrazole derivatives are known for various biological activities, including anti-inflammatory and analgesic properties. Additionally, the bromine atom can serve as a useful handle for further chemical modifications, making it a versatile intermediate in synthetic chemistry. Safety and handling precautions should be observed, as with all chemical substances, particularly those with potential biological activity.

5-amino-1-(4-bromophenyl)-1H-pyrazole-4-carboxylic acid

438243-87-9: 5-Amino-1-(4-bromophenyl)-1H-pyrazole-4-carboxylic acid is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), contributing to its potential as a biologically active molecule. The presence of the 4-bromophenyl substituent enhances its lipophilicity and may influence its interaction with biological targets. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid functionality. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as pyrazole derivatives are known for various biological activities, including anti-inflammatory and analgesic properties. Additionally, the bromine atom can serve as a useful handle for further chemical modifications, making it a versatile intermediate in synthetic chemistry. Safety and handling precautions should be observed, as with all chemical substances, particularly those with potential biological activity.

CAS 438243-87-9

5-amino-1-(4-bromophenyl)-1H-pyrazole-4-carboxylic acid

5-Amino-1-(4-bromophenyl)-1H-pyrazole-4-carboxylic acid

Ref: IN-DA00DCIG

5-Amino-1-(4-bromophenyl)-1H-pyrazole-4-carboxylic acid

Ref: 54-OR103641

5-AMINO-1-(4-BROMOPHENYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID

Ref: 10-F301523