3-(4-Chlorophenyl)-1H-pyrazol-5-amine, with the CAS number 78583-81-0, is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two adjacent nitrogen atoms. This compound features a 4-chlorophenyl group, indicating the presence of a chlorine atom attached to a phenyl ring at the para position relative to the pyrazole structure. The amine functional group at the 5-position of the pyrazole contributes to its reactivity and potential applications in medicinal chemistry. Typically, compounds of this nature may exhibit biological activity, making them of interest in drug development and research. The presence of the chlorophenyl moiety can influence the compound's lipophilicity and interaction with biological targets. Additionally, the compound's solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups. Overall, 3-(4-chlorophenyl)-1H-pyrazol-5-amine is a versatile compound with potential applications in various fields, including pharmaceuticals and agrochemicals.

3-(4-chlorophenyl)-1H-pyrazol-5-amine

78583-81-0: 5-(4-chlorophenyl)-1H-pyrazol-3-amine

5-(4-Chlorophenyl)-1H-pyrazol-3-amine

3-Amino-5-(4-chlorophenyl)pyrazole

5-Amino-3-(4-chlorophenyl)-1H-pyrazole

5-Amino-3-(4-chlorophenyl)pyrazole is an isomeric compound that yields ethanol in the presence of hydrochloric acid. The compound has centrosymmetric, tricyclic interactions, and dimers with benzaldehydes and other ring systems. 5-Amino-3-(4-chlorophenyl)pyrazole has a linear and heteroaromatic structure that allows for hydrogen bonding and stacking.

CAS 78583-81-0: 3-(4-chlorophenyl)-1H-pyrazol-5-amine

5-(4-Chlorophenyl)-1H-pyrazol-3-amine

Ref: IN-DA008MH2

3-Amino-5-(4-chlorophenyl)pyrazole

Ref: 3B-A2952

5-Amino-3-(4-chlorophenyl)-1H-pyrazole

Ref: 54-OR4080

5-Amino-3-(4-chlorophenyl)pyrazole

Ref: 3D-FA53872

5-(4-Chlorophenyl)-2H-pyrazol-3-ylamine

Ref: 10-F019533