5-Bromo-3-quinolinamine is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 5-position and an amino group at the 3-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the amino group, which can engage in hydrogen bonding. Its molecular structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. The bromine substituent can also influence its reactivity, potentially allowing for further functionalization through electrophilic substitution reactions. Additionally, 5-Bromo-3-quinolinamine may exhibit fluorescence properties, which can be useful in various analytical applications. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, this compound represents a versatile building block in organic synthesis and pharmaceutical research.

5-Bromo-3-quinolinamine

1330754-37-4: 5-Bromo-3-quinolinamine is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 5-position and an amino group at the 3-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the amino group, which can engage in hydrogen bonding. Its molecular structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. The bromine substituent can also influence its reactivity, potentially allowing for further functionalization through electrophilic substitution reactions. Additionally, 5-Bromo-3-quinolinamine may exhibit fluorescence properties, which can be useful in various analytical applications. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, this compound represents a versatile building block in organic synthesis and pharmaceutical research.

CAS 1330754-37-4

5-Bromo-3-quinolinamine

3-Quinolinamine, 5-bromo-

Ref: IN-DA00147C

5-Bromoquinolin-3-amine

Ref: 54-OR1061927

5-BROMOQUINOLIN-3-AMINE

Ref: 10-F305810