7-Chloro-2-methyl-3-(5-methyl-2-pyridinyl)-4(3H)-quinazolinone is a synthetic organic compound characterized by its quinazolinone core structure, which is a bicyclic compound containing both a benzene and a pyrimidine ring. This compound features a chlorine atom at the 7-position and a methyl group at the 2-position of the quinazolinone ring, along with a 5-methyl-2-pyridinyl substituent at the 3-position. The presence of these functional groups contributes to its potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The compound is likely to exhibit specific solubility and stability characteristics influenced by its molecular structure. Additionally, its CAS number, 338794-16-4, allows for precise identification and retrieval of information regarding its properties, safety data, and potential applications in research and industry. As with many quinazolinone derivatives, it may possess various pharmacological properties, including anti-inflammatory or anticancer activities, warranting further investigation.

7-CHLORO-2-METHYL-3-(5-METHYL-2-PYRIDINYL)-4(3H)-QUINAZOLINONE

338794-16-4: 7-Chloro-2-methyl-3-(5-methyl-2-pyridinyl)-4(3H)-quinazolinone is a synthetic organic compound characterized by its quinazolinone core structure, which is a bicyclic compound containing both a benzene and a pyrimidine ring. This compound features a chlorine atom at the 7-position and a methyl group at the 2-position of the quinazolinone ring, along with a 5-methyl-2-pyridinyl substituent at the 3-position. The presence of these functional groups contributes to its potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The compound is likely to exhibit specific solubility and stability characteristics influenced by its molecular structure. Additionally, its CAS number, 338794-16-4, allows for precise identification and retrieval of information regarding its properties, safety data, and potential applications in research and industry. As with many quinazolinone derivatives, it may possess various pharmacological properties, including anti-inflammatory or anticancer activities, warranting further investigation.

7-Chloro-2-methyl-3-(5-methylpyridin-2-yl)quinazolin-4(3H)-one

CAS 338794-16-4

7-CHLORO-2-METHYL-3-(5-METHYL-2-PYRIDINYL)-4(3H)-QUINAZOLINONE

7-Chloro-2-methyl-3-(5-methylpyridin-2-yl)quinazolin-4(3H)-one

Ref: 54-OR93695

7-Chloro-2-methyl-3-(5-methylpyridin-2-yl)quinazolin-4(3H)-one

Ref: 10-F982837