1-(2-Fluorophenyl)-1H-pyrazole is an organic compound characterized by its pyrazole ring, which is a five-membered aromatic heterocycle containing two nitrogen atoms. The presence of a fluorophenyl group at the 1-position of the pyrazole ring contributes to its unique chemical properties, including potential variations in reactivity and biological activity due to the electronegative fluorine atom. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water, reflecting its hydrophobic characteristics. It is often utilized in medicinal chemistry and research due to its potential as a pharmacophore, with applications in developing therapeutic agents. The compound's structure allows for various substitution patterns, which can influence its biological interactions and efficacy. Additionally, 1-(2-fluorophenyl)-1H-pyrazole may undergo typical organic reactions, such as electrophilic aromatic substitution, making it a versatile building block in synthetic organic chemistry. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity and environmental impact.

1-(2-fluorophenyl)-1H-pyrazole

35715-66-3: 1-(2-Fluorophenyl)-1H-pyrazole is an organic compound characterized by its pyrazole ring, which is a five-membered aromatic heterocycle containing two nitrogen atoms. The presence of a fluorophenyl group at the 1-position of the pyrazole ring contributes to its unique chemical properties, including potential variations in reactivity and biological activity due to the electronegative fluorine atom. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water, reflecting its hydrophobic characteristics. It is often utilized in medicinal chemistry and research due to its potential as a pharmacophore, with applications in developing therapeutic agents. The compound's structure allows for various substitution patterns, which can influence its biological interactions and efficacy. Additionally, 1-(2-fluorophenyl)-1H-pyrazole may undergo typical organic reactions, such as electrophilic aromatic substitution, making it a versatile building block in synthetic organic chemistry. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity and environmental impact.

CAS 35715-66-3

1-(2-fluorophenyl)-1H-pyrazole

1-(2-Fluorophenyl)-1H-pyrazole

Ref: IN-DA00C0ZW

1-(2-Fluorophenyl)-1H-pyrazole

Ref: 54-PC902185