4-Fluoro-2,3-dihydro-1H-indole 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 4-position of the indole ring influences its electronic properties and reactivity. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents. Its molecular formula reflects the presence of carbon, hydrogen, and fluorine atoms, contributing to its unique chemical behavior. The dihydro form indicates that it has two hydrogen atoms added to the indole structure, which can affect its stability and reactivity. 4-Fluoro-2,3-dihydro-1H-indole is of interest in medicinal chemistry and drug development due to its potential biological activity, including interactions with various biological targets. Its synthesis and characterization are important for exploring its applications in pharmaceuticals and materials science. As with many fluorinated compounds, it may exhibit enhanced metabolic stability and lipophilicity, making it a valuable candidate for further research.

4-fluoro-2,3-dihydro-1H-indole

552866-98-5: 4-Fluoro-2,3-dihydro-1H-indole 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 4-position of the indole ring influences its electronic properties and reactivity. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents. Its molecular formula reflects the presence of carbon, hydrogen, and fluorine atoms, contributing to its unique chemical behavior. The dihydro form indicates that it has two hydrogen atoms added to the indole structure, which can affect its stability and reactivity. 4-Fluoro-2,3-dihydro-1H-indole is of interest in medicinal chemistry and drug development due to its potential biological activity, including interactions with various biological targets. Its synthesis and characterization are important for exploring its applications in pharmaceuticals and materials science. As with many fluorinated compounds, it may exhibit enhanced metabolic stability and lipophilicity, making it a valuable candidate for further research.

CAS 552866-98-5

4-fluoro-2,3-dihydro-1H-indole

4-FLUORO-2,3-DIHYDRO-1H-INDOLE HYDROCHLORIDE

Ref: IN-DA00DBT6

4-Fluoroindoline

Ref: 54-PC49192

4-Fluoroindoline

Ref: 10-F219978