Ethyl 1-cyclopropyl-4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate, identified by its CAS number 423768-53-0, is a chemical compound that belongs to the class of pyrrole derivatives. This compound features a pyrrole ring, which is a five-membered aromatic heterocycle containing nitrogen. The presence of a cyclopropyl group and various substituents, such as a formyl group and ethyl ester, contributes to its unique chemical properties and potential reactivity. Typically, compounds of this nature exhibit interesting biological activities, making them of interest in medicinal chemistry and drug development. The ethyl ester functional group suggests that it may undergo hydrolysis to yield the corresponding carboxylic acid, which can further participate in various chemical reactions. Additionally, the structural complexity and the presence of multiple functional groups may influence its solubility, stability, and interaction with biological targets. Overall, this compound exemplifies the diverse chemistry associated with pyrrole derivatives and their potential applications in various fields.

ethyl 1-cyclopropyl-4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate

423768-53-0: Ethyl 1-cyclopropyl-4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate, identified by its CAS number 423768-53-0, is a chemical compound that belongs to the class of pyrrole derivatives. This compound features a pyrrole ring, which is a five-membered aromatic heterocycle containing nitrogen. The presence of a cyclopropyl group and various substituents, such as a formyl group and ethyl ester, contributes to its unique chemical properties and potential reactivity. Typically, compounds of this nature exhibit interesting biological activities, making them of interest in medicinal chemistry and drug development. The ethyl ester functional group suggests that it may undergo hydrolysis to yield the corresponding carboxylic acid, which can further participate in various chemical reactions. Additionally, the structural complexity and the presence of multiple functional groups may influence its solubility, stability, and interaction with biological targets. Overall, this compound exemplifies the diverse chemistry associated with pyrrole derivatives and their potential applications in various fields.

<p>Ethyl 1-cyclopropyl-4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate</p>

CAS 423768-53-0

ethyl 1-cyclopropyl-4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate

Ethyl 1-cyclopropyl-4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate

Ref: 54-OR25975