4-Chloro-2,5-dimethylquinazoline is a heterocyclic organic compound characterized by its quinazoline structure, which consists of a fused benzene and pyrimidine ring. The presence of chlorine at the 4-position and two methyl groups at the 2 and 5 positions 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 nature. It is often used in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. The chlorine substituent can influence the compound's reactivity and biological activity, making it a subject of interest in medicinal chemistry. Additionally, the presence of methyl groups can affect the compound's steric and electronic properties, potentially impacting its interactions with biological targets. As with many quinazoline derivatives, 4-Chloro-2,5-dimethylquinazoline may exhibit various pharmacological activities, including antitumor and antimicrobial properties, although specific biological data would depend on experimental studies.

4-Chloro-2,5-dimethylquinazoline

147006-57-3: Quinazoline, 4-chloro-2,5-dimethyl-, 4-Chloro-2,5-dimethylquinazoline

CAS 147006-57-3: 4-Chloro-2,5-dimethylquinazoline

4-Chloro-2,5-dimethylquinazoline

Ref: 10-F781589

4-Chloro-2,5-dimethylquinazoline

Ref: 3D-XFA00657

Quinazoline, 4-chloro-2,5-dimethyl-

Ref: IN-DA001EIS

4-Chloro-2,5-dimethylquinazoline

Ref: 54-OR85968