CAS 1134334-43-2

5-Ethoxy-1-propyl-1H-indole-3-carboxaldehyde

Description:

5-Ethoxy-1-propyl-1H-indole-3-carboxaldehyde 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 particular compound features an ethoxy group and a propyl group attached to the indole nitrogen, along with a carboxaldehyde functional group at the 3-position of the indole. The presence of the ethoxy and propyl substituents contributes to its hydrophobic characteristics, while the aldehyde group introduces reactivity typical of carbonyl compounds, making it susceptible to nucleophilic attack. This compound may exhibit biological activity, potentially influencing various biochemical pathways, although specific biological properties would require empirical investigation. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. As with many indole derivatives, it may also serve as a scaffold for further chemical modifications, enhancing its utility in synthetic organic chemistry. Safety and handling precautions should be observed due to the reactive nature of the aldehyde group.

Formula: C₁₄H₁₇NO₂

InChI: InChI=1S/C14H17NO2/c1-3-7-15-9-11(10-16)13-8-12(17-4-2)5-6-14(13)15/h5-6,8-10H,3-4,7H2,1-2H3

InChI key: InChIKey=JYDKVFPUDYMXFR-UHFFFAOYSA-N

SMILES: C(CC)N1C=2C(C(C=O)=C1)=CC(OCC)=CC2

Synonyms:

• 1H-Indole-3-carboxaldehyde, 5-ethoxy-1-propyl-
• 5-Ethoxy-1-propyl-1H-indole-3-carboxaldehyde