1-[4-(Dimethylamino)phenyl]-2,5-dimethyl-1H-pyrrole-3-carbaldehyde, with the CAS number 32570-93-7, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a dimethylamino group, which is known for its electron-donating properties, enhancing the compound's reactivity and solubility in various solvents. The presence of the aldehyde functional group contributes to its potential as a reactive intermediate in organic synthesis, particularly in the formation of imines and other derivatives. The dimethyl and phenyl substituents on the pyrrole ring can influence its electronic properties and steric hindrance, affecting its behavior in chemical reactions. This compound may exhibit fluorescence and has potential applications in dye chemistry and materials science. As with many organic compounds, its stability, solubility, and reactivity can vary based on environmental conditions such as temperature and pH. Safety data should be consulted for handling and usage, as compounds with similar structures can exhibit varying levels of toxicity.

1-[4-(dimethylamino)phenyl]-2,5-dimethyl-1H-pyrrole-3-carbaldehyde

32570-93-7: 1-[4-(Dimethylamino)phenyl]-2,5-dimethyl-1H-pyrrole-3-carbaldehyde, with the CAS number 32570-93-7, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a dimethylamino group, which is known for its electron-donating properties, enhancing the compound's reactivity and solubility in various solvents. The presence of the aldehyde functional group contributes to its potential as a reactive intermediate in organic synthesis, particularly in the formation of imines and other derivatives. The dimethyl and phenyl substituents on the pyrrole ring can influence its electronic properties and steric hindrance, affecting its behavior in chemical reactions. This compound may exhibit fluorescence and has potential applications in dye chemistry and materials science. As with many organic compounds, its stability, solubility, and reactivity can vary based on environmental conditions such as temperature and pH. Safety data should be consulted for handling and usage, as compounds with similar structures can exhibit varying levels of toxicity.

CAS 32570-93-7

1-[4-(dimethylamino)phenyl]-2,5-dimethyl-1H-pyrrole-3-carbaldehyde

1-[4-(dimethylamino)phenyl]-2,5-dimethyl-1H-pyrrole-3-carbaldehyde

Ref: 10-F314986