4-Chloroquinolin-2-amine is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the 4-position and an amino group at the 2-position contributes to its unique chemical properties. This compound typically appears as a solid and is known for its potential biological activity, making it of interest in medicinal chemistry and drug development. It may exhibit properties such as antimicrobial or antitumor activity, although specific biological effects can vary based on structural modifications and the presence of other functional groups. The compound is soluble in organic solvents and may have limited solubility in water, which is common for many nitrogen-containing heterocycles. Its reactivity can be influenced by the amino and chloro substituents, allowing for further chemical modifications. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken during use and experimentation.

4-chloroquinolin-2-amine

2-Quinolinamine, 4-chloro-

4-Chloroquinolin-2-amine

4-Chloroquinolin-2-amine is a noncatalytic, palladium-catalyzed process for the synthesis of amines from 2-chloroquinoline and adamantane. This reaction results in the substitution of the chloro group on the 2-chloroquinoline with an amino group. The yield for this reaction is high, however it does not work with other substituents on the 2-chloroquinoline. 4-Chloroquinolin-2-amine can be used in reactions that require amines without substituents such as amination or arylation.

CAS 20151-42-2: 4-chloroquinolin-2-amine

2-Quinolinamine, 4-chloro-

Ref: IN-DA002DGK

4-Chloroquinolin-2-amine

Ref: 10-F618905

4-Chloroquinolin-2-amine

Ref: 3D-FC142824