7-Bromo-4-fluoro-1H-indole is a heterocyclic organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of bromine and fluorine substituents at the 7 and 4 positions, respectively, significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to brownish color and is soluble in organic solvents. It is often used in medicinal chemistry and research due to its potential biological activity, particularly in the development of pharmaceuticals. The bromine atom can participate in electrophilic substitution reactions, while the fluorine atom can enhance the compound's lipophilicity and metabolic stability. Additionally, 7-bromo-4-fluoro-1H-indole may exhibit interesting photophysical properties, making it a candidate for applications in materials science and organic electronics. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, this compound serves as a valuable building block in synthetic organic chemistry and drug discovery.

7-bromo-4-fluoro-1H-indole

292636-09-0: 1H-indole, 7-bromo-4-fluoro-,  7-Bromo-4-fluoro-1H-indole

7-Bromo-4-fluoro-1H-indole is a potent inhibitor of plasma concentrations of indole and has been shown to enhance plasma exposure. It is an analog of the compound 7-bromoindole, which is used as a prodrug for the oral bioavailability of the potent HIV-1 inhibitor atazanavir. The drug is a synthetic compound that inhibits human immunodeficiency virus type 1 (HIV-1) replication by inhibiting reverse transcriptase.

CAS 292636-09-0: 7-bromo-4-fluoro-1H-indole

7-Bromo-4-fluoro-1H-indole

Ref: 3D-FB144369

7-Bromo-4-fluoro-1H-indole

Ref: 10-F219746

1H-Indole, 7-bromo-4-fluoro-

Ref: IN-DA002XW8

7-Bromo-4-fluoro-1H-indole

Ref: 54-PC7088