1H-Indol-4-ol, 5-ethoxy- (CAS 130570-26-2) is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a hydroxyl group (-OH) at the 4-position and an ethoxy group (-OCH2CH3) at the 5-position of the indole ring, contributing to its unique chemical properties. The presence of the hydroxyl group imparts potential for hydrogen bonding, influencing its solubility and reactivity. The ethoxy group enhances the lipophilicity of the molecule, which may affect its biological activity and interaction with other substances. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry and drug development. Additionally, its structural features suggest potential applications in organic synthesis and material science. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic substitutions and coupling reactions, making it a versatile building block in organic synthesis.

1H-Indol-4-ol, 5-ethoxy-

130570-26-2: 1H-Indol-4-ol, 5-ethoxy- (CAS 130570-26-2) is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a hydroxyl group (-OH) at the 4-position and an ethoxy group (-OCH2CH3) at the 5-position of the indole ring, contributing to its unique chemical properties. The presence of the hydroxyl group imparts potential for hydrogen bonding, influencing its solubility and reactivity. The ethoxy group enhances the lipophilicity of the molecule, which may affect its biological activity and interaction with other substances. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry and drug development. Additionally, its structural features suggest potential applications in organic synthesis and material science. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic substitutions and coupling reactions, making it a versatile building block in organic synthesis.

CAS 130570-26-2

1H-Indol-4-ol, 5-ethoxy-

5-Ethoxy-1H-indol-4-ol

Ref: IN-DA000UN3

5-Ethoxy-1H-indol-4-ol

Ref: 54-OR305528