1-[(4-Nitrophenyl)methyl]-1H-pyrazole is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two adjacent nitrogen atoms. The presence of a 4-nitrophenyl group attached to the pyrazole structure significantly influences its chemical properties and reactivity. This compound typically exhibits a yellow crystalline appearance due to the nitro group, which is known for its electron-withdrawing properties, enhancing the compound's electrophilicity. It is often utilized in various fields, including medicinal chemistry and agrochemicals, due to its potential biological activities. The compound may exhibit properties such as moderate solubility in organic solvents and limited solubility in water, which is common for many pyrazole derivatives. Additionally, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, owing to the functional groups present. Safety data should be consulted for handling, as nitro compounds can pose health risks. Overall, 1-[(4-Nitrophenyl)methyl]-1H-pyrazole is a versatile compound with significant implications in research and application.

1-[(4-Nitrophenyl)methyl]-1H-pyrazole

110525-57-0: 1-[(4-Nitrophenyl)methyl]-1H-pyrazole, 1H-Pyrazole, 1-[(4-nitrophenyl)methyl]-, 1-[(4-Nitrophenyl)methyl]pyrazole

1-(4-Nitrobenzyl)-1H-pyrazole

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CAS 110525-57-0: 1-[(4-Nitrophenyl)methyl]-1H-pyrazole

1-(4-Nitrobenzyl)-1H-pyrazole

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1-(4-Nitrobenzyl)-1H-pyrazole

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1-(4-Nitrobenzyl)-1H-pyrazole

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