3-(4-Bromophenyl)-1H-pyrazole is an organic compound characterized by its pyrazole ring structure substituted with a bromophenyl group. It typically appears as a solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The presence of the bromine atom enhances its reactivity and can influence its interaction with biological targets. This compound is often utilized in research settings, particularly in studies related to anti-inflammatory and anticancer properties. It has a molecular formula that reflects its composition of carbon, hydrogen, and bromine atoms, and it is generally handled with standard laboratory safety precautions due to its chemical nature. The purity of 97% indicates a high level of refinement, making it suitable for various experimental applications. As with many organic compounds, it is important to consider its solubility, stability, and reactivity under different conditions when working with it in the laboratory.

3-(4-BROMOPHENYL)-1H-PYRAZOLE, 97%

73387-46-9: 3-(4-Bromophenyl)-1H-pyrazole is an organic compound characterized by its pyrazole ring structure substituted with a bromophenyl group. It typically appears as a solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The presence of the bromine atom enhances its reactivity and can influence its interaction with biological targets. This compound is often utilized in research settings, particularly in studies related to anti-inflammatory and anticancer properties. It has a molecular formula that reflects its composition of carbon, hydrogen, and bromine atoms, and it is generally handled with standard laboratory safety precautions due to its chemical nature. The purity of 97% indicates a high level of refinement, making it suitable for various experimental applications. As with many organic compounds, it is important to consider its solubility, stability, and reactivity under different conditions when working with it in the laboratory.

CAS 73387-46-9

3-(4-BROMOPHENYL)-1H-PYRAZOLE, 97%

3-(4-Bromophenyl)-1H-pyrazole

Ref: IN-DA005EEJ

3-(4-Bromophenyl)-1H-pyrazole

Ref: 54-OR21

3-(4-Bromophenyl)-1H-pyrazole

Ref: 10-F033608