2-Chloro-N-methylquinazolin-4-amine is a chemical compound characterized by its quinazoline core structure, which is a bicyclic compound containing two fused aromatic rings. The presence of a chlorine atom at the second position and a methylamino group at the fourth position contributes to its unique reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of functional groups that can interact with biological targets. The chlorine substituent can influence the compound's lipophilicity and biological activity, while the N-methyl group may affect its pharmacokinetic properties. As with many quinazoline derivatives, 2-chloro-N-methylquinazolin-4-amine may exhibit various biological activities, including antitumor or antimicrobial properties, making it of interest in drug discovery and development. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

2-chloro-N-methylquinazolin-4-amine

83260-68-8: 2-Chloro-N-methylquinazolin-4-amine is a chemical compound characterized by its quinazoline core structure, which is a bicyclic compound containing two fused aromatic rings. The presence of a chlorine atom at the second position and a methylamino group at the fourth position contributes to its unique reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of functional groups that can interact with biological targets. The chlorine substituent can influence the compound's lipophilicity and biological activity, while the N-methyl group may affect its pharmacokinetic properties. As with many quinazoline derivatives, 2-chloro-N-methylquinazolin-4-amine may exhibit various biological activities, including antitumor or antimicrobial properties, making it of interest in drug discovery and development. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

CAS 83260-68-8

2-chloro-N-methylquinazolin-4-amine

2-chloro-N-methylquinazolin-4-amine

Ref: IN-DA00JAVD

2-Chloro-N-methylquinazolin-4-amine

Ref: 3D-IDA26068