5-Bromo-1-[2-oxo-2-(pyrrolidin-1-yl)ethyl]-1H-indole-3-carbaldehyde is a synthetic organic compound characterized by its complex structure, which includes an indole ring, a bromine substituent, and a pyrrolidine moiety. The presence of the aldehyde functional group contributes to its reactivity, making it useful in various chemical reactions, including condensation and substitution reactions. The compound's molecular structure suggests potential biological activity, which may be explored in medicinal chemistry, particularly in the development of pharmaceuticals. Its bromine atom may enhance lipophilicity and influence the compound's interaction with biological targets. Additionally, the oxo group and the pyrrolidine ring can contribute to the compound's overall stability and solubility in organic solvents. As with many indole derivatives, this compound may exhibit interesting properties such as fluorescence or photochemical behavior, which can be advantageous in research applications. Safety and handling precautions should be observed due to the presence of reactive functional groups and the potential for biological activity.

5-bromo-1-[2-oxo-2-(pyrrolidin-1-yl)ethyl]-1H-indole-3-carbaldehyde

434299-46-4: 5-Bromo-1-[2-oxo-2-(pyrrolidin-1-yl)ethyl]-1H-indole-3-carbaldehyde is a synthetic organic compound characterized by its complex structure, which includes an indole ring, a bromine substituent, and a pyrrolidine moiety. The presence of the aldehyde functional group contributes to its reactivity, making it useful in various chemical reactions, including condensation and substitution reactions. The compound's molecular structure suggests potential biological activity, which may be explored in medicinal chemistry, particularly in the development of pharmaceuticals. Its bromine atom may enhance lipophilicity and influence the compound's interaction with biological targets. Additionally, the oxo group and the pyrrolidine ring can contribute to the compound's overall stability and solubility in organic solvents. As with many indole derivatives, this compound may exhibit interesting properties such as fluorescence or photochemical behavior, which can be advantageous in research applications. Safety and handling precautions should be observed due to the presence of reactive functional groups and the potential for biological activity.

CAS 434299-46-4

5-bromo-1-[2-oxo-2-(pyrrolidin-1-yl)ethyl]-1H-indole-3-carbaldehyde

5-bromo-1-(2-oxo-2-pyrrolidin-1-ylethyl)-1H-indole-3-carbaldehyde

Ref: 10-F315314