5,7-Dinitrooxindole is a chemical compound characterized by its oxindole structure, which features a bicyclic framework consisting of a benzene ring fused to a pyrrolidine ring. The presence of two nitro groups at the 5 and 7 positions of the oxindole moiety significantly influences its chemical properties, including its reactivity and potential biological activity. This compound is typically a yellow crystalline solid, indicating the presence of nitro groups, which often impart distinctive colors to organic compounds. 5,7-Dinitrooxindole is of interest in various fields, including medicinal chemistry, due to its potential pharmacological properties. The nitro groups can participate in electrophilic substitution reactions, making the compound a versatile intermediate in organic synthesis. Additionally, the compound may exhibit interesting interactions with biological targets, which could be explored for therapeutic applications. However, handling and usage should be approached with caution due to the potential toxicity associated with nitro compounds.

5,7-Dinitrooxindole

30490-21-2: 5,7-dinitro-1,3-dihydro-2H-indol-2-one

5,7-Dinitrooxindole is an oxindole that has been synthesized by the ring-opening of hydroxylated triazoles. It has a hydrophobic character due to the presence of two nitro groups in the molecule. This compound can be used as a synthetic precursor for other compounds with biological activity. 5,7-Dinitrooxindole can be oxidized with hydroxide ions to yield 7-hydroxy-5,6-dinitrooxindole, which is an optical isomer of the molecule. The conformation of 5,7-dinitrooxindole can be transferred to other molecules using amines and cyclic sulfoxides.

CAS 30490-21-2: 5,7-Dinitrooxindole

5,7-Dinitrooxindole

Ref: 3D-FD147713

2H-Indol-2-one, 1,3-dihydro-5,7-dinitro-

Ref: IN-DA0030CB

5,7-Dinitro-2-oxindole

Ref: 54-OR10464