4-Quinolinamine, N-methyl- is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. This compound features an amino group (-NH2) at the 4-position of the quinoline ring and a methyl group attached to the nitrogen atom, making it a derivative of quinoline. It is typically a yellow to brown solid and is soluble in organic solvents. The presence of the amino group allows for potential reactivity, including the ability to form salts and participate in various chemical reactions, such as alkylation and acylation. This compound may exhibit biological activity, making it of interest in medicinal chemistry and pharmacology. Its properties, such as melting point, boiling point, and spectral characteristics, can vary based on purity and specific conditions. As with many nitrogen-containing heterocycles, it may also display interesting electronic properties, which can be leveraged in various applications, including dye synthesis and as a building block in organic synthesis. Safety data should be consulted for handling and usage guidelines.

4-Quinolinamine, N-methyl-

16401-66-4: 4-Quinolinamine, N-methyl- is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. This compound features an amino group (-NH2) at the 4-position of the quinoline ring and a methyl group attached to the nitrogen atom, making it a derivative of quinoline. It is typically a yellow to brown solid and is soluble in organic solvents. The presence of the amino group allows for potential reactivity, including the ability to form salts and participate in various chemical reactions, such as alkylation and acylation. This compound may exhibit biological activity, making it of interest in medicinal chemistry and pharmacology. Its properties, such as melting point, boiling point, and spectral characteristics, can vary based on purity and specific conditions. As with many nitrogen-containing heterocycles, it may also display interesting electronic properties, which can be leveraged in various applications, including dye synthesis and as a building block in organic synthesis. Safety data should be consulted for handling and usage guidelines.

CAS 16401-66-4

4-Quinolinamine, N-methyl-

N-methylquinolin-4-amine

Ref: IN-DA00AQT0

N-methylquinolin-4-amine

Ref: 54-OR93604

N-methylquinolin-4-amine

Ref: 10-F731348