1-(4-Bromophenyl)pyrrolidine-2,5-dione, identified by its CAS number 41167-74-2, is a chemical compound characterized by its unique structure, which includes a pyrrolidine ring substituted with a bromophenyl group and two carbonyl groups. This compound typically exhibits properties associated with both the pyrrolidine and the aromatic bromophenyl moieties, such as potential reactivity due to the presence of the carbonyl groups, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. The bromine atom in the para position of the phenyl ring can influence the compound's electronic properties, potentially enhancing its reactivity and solubility in organic solvents. Additionally, the presence of the pyrrolidine ring may impart certain biological activities, making it of interest in medicinal chemistry. Overall, this compound's characteristics, including its molecular structure, reactivity, and potential applications, make it a subject of interest in both synthetic and medicinal chemistry research.

1-(4-bromophenyl)pyrrolidine-2,5-dione

41167-74-2: 1-(4-Bromophenyl)pyrrolidine-2,5-dione, identified by its CAS number 41167-74-2, is a chemical compound characterized by its unique structure, which includes a pyrrolidine ring substituted with a bromophenyl group and two carbonyl groups. This compound typically exhibits properties associated with both the pyrrolidine and the aromatic bromophenyl moieties, such as potential reactivity due to the presence of the carbonyl groups, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. The bromine atom in the para position of the phenyl ring can influence the compound's electronic properties, potentially enhancing its reactivity and solubility in organic solvents. Additionally, the presence of the pyrrolidine ring may impart certain biological activities, making it of interest in medicinal chemistry. Overall, this compound's characteristics, including its molecular structure, reactivity, and potential applications, make it a subject of interest in both synthetic and medicinal chemistry research.

CAS 41167-74-2

1-(4-bromophenyl)pyrrolidine-2,5-dione

N-(4-Bromophenyl)succinimide

Ref: 10-F021870