1-Ethylindole-4-carbaldehyde 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 an ethyl group attached to the nitrogen atom of the indole, as well as a formyl group (-CHO) at the 4-position of the indole ring, contributing to its reactivity and potential applications in organic synthesis. It is typically a yellow to brown liquid or solid, depending on its purity and specific conditions. The presence of the aldehyde functional group makes it susceptible to oxidation and nucleophilic attack, which can be exploited in various chemical reactions, including condensation and addition reactions. 1-Ethylindole-4-carbaldehyde may also exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its unique structure allows for potential interactions with biological targets, which can be investigated further in pharmacological studies. As with many organic compounds, proper handling and storage are essential to maintain its stability and prevent degradation.

1-ethylindole-4-carbaldehyde

894852-86-9: 1-Ethylindole-4-carbaldehyde 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 an ethyl group attached to the nitrogen atom of the indole, as well as a formyl group (-CHO) at the 4-position of the indole ring, contributing to its reactivity and potential applications in organic synthesis. It is typically a yellow to brown liquid or solid, depending on its purity and specific conditions. The presence of the aldehyde functional group makes it susceptible to oxidation and nucleophilic attack, which can be exploited in various chemical reactions, including condensation and addition reactions. 1-Ethylindole-4-carbaldehyde may also exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its unique structure allows for potential interactions with biological targets, which can be investigated further in pharmacological studies. As with many organic compounds, proper handling and storage are essential to maintain its stability and prevent degradation.

CAS 894852-86-9

1-ethylindole-4-carbaldehyde

1-Ethyl-1H-indole-4-carbaldehyde

Ref: IN-DA0041WN

1-Ethyl-1H-indole-4-carbaldehyde

Ref: 54-OR926423

1-ethyl-1H-indole-4-carbaldehyde

Ref: 10-F310955