Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate, with the CAS number 132414-78-9, is a chemical compound characterized by its complex bicyclic structure, which includes a pyrrole and a hexahydropyrrole moiety. This compound typically exhibits properties associated with both heterocyclic and aliphatic compounds, including potential solubility in organic solvents and moderate stability under standard conditions. Its structure suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, due to the presence of functional groups like the carboxylate ester. Ethyl esters often display moderate volatility and can be involved in esterification and hydrolysis reactions. The presence of the benzyl group may enhance its lipophilicity, potentially influencing its biological activity and interactions with other molecules. While specific physical properties such as melting point, boiling point, and density are not provided, compounds of this nature often find applications in medicinal chemistry and materials science due to their unique structural features.

ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate

132414-78-9: Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate, with the CAS number 132414-78-9, is a chemical compound characterized by its complex bicyclic structure, which includes a pyrrole and a hexahydropyrrole moiety. This compound typically exhibits properties associated with both heterocyclic and aliphatic compounds, including potential solubility in organic solvents and moderate stability under standard conditions. Its structure suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, due to the presence of functional groups like the carboxylate ester. Ethyl esters often display moderate volatility and can be involved in esterification and hydrolysis reactions. The presence of the benzyl group may enhance its lipophilicity, potentially influencing its biological activity and interactions with other molecules. While specific physical properties such as melting point, boiling point, and density are not provided, compounds of this nature often find applications in medicinal chemistry and materials science due to their unique structural features.

CAS 132414-78-9

ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate

Pyrrolo[3,4-b]pyrrole-5(1H)-carboxylic acid, hexahydro-1-(phenylmethyl)-, ethyl ester

Ref: IN-DA0010NT