1,3-Dimethyl-4-nitro-1H-pyrazol-5-amine is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features two methyl groups at the 1 and 3 positions and a nitro group at the 4 position, along with an amino group at the 5 position of the pyrazole ring. The presence of these functional groups contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity and stability. Additionally, the compound's molecular structure suggests it may exhibit specific biological activities, making it of interest for research in medicinal chemistry. Its CAS number, 76689-64-0, allows for easy identification and reference in chemical databases. As with many nitrogen-containing heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and reductions, depending on the reaction conditions.

1,3-dimethyl-4-nitro-1H-pyrazol-5-amine

76689-64-0: 1,3-Dimethyl-4-nitro-1H-pyrazol-5-amine is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features two methyl groups at the 1 and 3 positions and a nitro group at the 4 position, along with an amino group at the 5 position of the pyrazole ring. The presence of these functional groups contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity and stability. Additionally, the compound's molecular structure suggests it may exhibit specific biological activities, making it of interest for research in medicinal chemistry. Its CAS number, 76689-64-0, allows for easy identification and reference in chemical databases. As with many nitrogen-containing heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and reductions, depending on the reaction conditions.

CAS 76689-64-0

1,3-dimethyl-4-nitro-1H-pyrazol-5-amine

1,3-Dimethyl-4-nitro-1H-pyrazol-5-amine

Ref: 3D-BDA68964