1H-Indole, 6-fluoro-4-methoxy- is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a fluorine atom at the 6-position and a methoxy group at the 4-position contributes to its unique chemical properties. This compound is typically classified as a heterocyclic aromatic organic compound, exhibiting both aromaticity and basicity due to the nitrogen atom in the indole ring. It may display interesting biological activities, making it of interest in medicinal chemistry and drug development. The methoxy group can influence the compound's solubility and reactivity, while the fluorine atom can enhance metabolic stability and lipophilicity. Additionally, 1H-Indole derivatives are often studied for their potential applications in pharmaceuticals, agrochemicals, and materials science. As with many indole derivatives, this compound may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a versatile building block in organic synthesis.

1H-Indole, 6-fluoro-4-Methoxy-

885521-02-8: 1H-Indole, 6-fluoro-4-methoxy- is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a fluorine atom at the 6-position and a methoxy group at the 4-position contributes to its unique chemical properties. This compound is typically classified as a heterocyclic aromatic organic compound, exhibiting both aromaticity and basicity due to the nitrogen atom in the indole ring. It may display interesting biological activities, making it of interest in medicinal chemistry and drug development. The methoxy group can influence the compound's solubility and reactivity, while the fluorine atom can enhance metabolic stability and lipophilicity. Additionally, 1H-Indole derivatives are often studied for their potential applications in pharmaceuticals, agrochemicals, and materials science. As with many indole derivatives, this compound may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a versatile building block in organic synthesis.

CAS 885521-02-8

1H-Indole, 6-fluoro-4-Methoxy-

6-Fluoro-4-methoxy-1H-indole

Ref: IN-DA00IF6X

6-Fluoro-4-methoxy-1H-indole

Ref: 54-PC1006380