2-Ethyl 5-methyl 1H-indole-2,5-dicarboxylate is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features two carboxylate ester functional groups, contributing to its reactivity and solubility properties. The presence of ethyl and methyl substituents on the indole ring influences its steric and electronic properties, potentially affecting its biological activity and interactions. Typically, compounds like this may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The molecular structure allows for various synthetic modifications, which can lead to derivatives with enhanced or altered properties. Additionally, the compound's solubility in organic solvents and stability under standard laboratory conditions are important characteristics for its handling and application in research. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic substitutions and cycloadditions, making it a versatile building block in organic synthesis.

2-ethyl 5-methyl 1H-indole-2,5-dicarboxylate

884494-66-0: 2-Ethyl 5-methyl 1H-indole-2,5-dicarboxylate is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features two carboxylate ester functional groups, contributing to its reactivity and solubility properties. The presence of ethyl and methyl substituents on the indole ring influences its steric and electronic properties, potentially affecting its biological activity and interactions. Typically, compounds like this may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The molecular structure allows for various synthetic modifications, which can lead to derivatives with enhanced or altered properties. Additionally, the compound's solubility in organic solvents and stability under standard laboratory conditions are important characteristics for its handling and application in research. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic substitutions and cycloadditions, making it a versatile building block in organic synthesis.

CAS 884494-66-0

2-ethyl 5-methyl 1H-indole-2,5-dicarboxylate

2-Ethyl 5-methyl 1H-indole-2,5-dicarboxylate

Ref: IN-DA004EME

2-Ethyl 5-methyl 1H-indole-2,5-dicarboxylate

Ref: 54-OR1046266

2-Ethyl 5-methyl 1H-indole-2,5-dicarboxylate

Ref: 10-F235413