7-Chloro-8-methyl-quinolin-4-amine is a chemical compound characterized by its quinoline structure, which consists of a bicyclic aromatic system. The presence of a chlorine atom at the 7-position and a methyl group at the 8-position, along with an amino group at the 4-position, contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic quinoline core. It is often studied for its potential biological activities, including antimicrobial and anticancer properties, owing to the reactivity of the amino group and the electron-withdrawing nature of the chlorine substituent. The compound's structure allows for various interactions with biological targets, making it of interest in medicinal chemistry. Additionally, its synthesis and characterization involve standard organic chemistry techniques, including nucleophilic substitution and functional group transformations. As with many quinoline derivatives, it may also exhibit fluorescence, which can be useful in analytical applications.

7-chloro-8-methyl-quinolin-4-amine

948293-41-2: 7-Chloro-8-methyl-quinolin-4-amine is a chemical compound characterized by its quinoline structure, which consists of a bicyclic aromatic system. The presence of a chlorine atom at the 7-position and a methyl group at the 8-position, along with an amino group at the 4-position, contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic quinoline core. It is often studied for its potential biological activities, including antimicrobial and anticancer properties, owing to the reactivity of the amino group and the electron-withdrawing nature of the chlorine substituent. The compound's structure allows for various interactions with biological targets, making it of interest in medicinal chemistry. Additionally, its synthesis and characterization involve standard organic chemistry techniques, including nucleophilic substitution and functional group transformations. As with many quinoline derivatives, it may also exhibit fluorescence, which can be useful in analytical applications.

CAS 948293-41-2

7-chloro-8-methyl-quinolin-4-amine

4-Amino-7-chloro-8-methylquinoline

Ref: 54-OR307951