7-(3-Hydroxypropoxy)quinazolin-4(3H)-one is a chemical compound characterized by its quinazolinone core, which is a bicyclic structure containing both a benzene and a pyrimidine ring. This compound features a hydroxypropoxy substituent at the 7-position, contributing to its solubility and potential biological activity. The presence of the hydroxy group enhances its ability to form hydrogen bonds, which may influence its interactions with biological targets. The compound is typically studied for its potential pharmacological properties, including anti-inflammatory and anticancer activities, owing to the structural motifs common in bioactive molecules. Its molecular structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and esterifications. Additionally, the compound's stability, solubility, and reactivity can be influenced by the functional groups present, making it a subject of interest in medicinal chemistry and drug development. As with many quinazolinone derivatives, it may exhibit a range of biological activities, warranting further investigation into its therapeutic potential.

7-(3-hydroxypropoxy)quinazolin-4(3H)-one

557770-89-5: 7-(3-Hydroxypropoxy)quinazolin-4(3H)-one is a chemical compound characterized by its quinazolinone core, which is a bicyclic structure containing both a benzene and a pyrimidine ring. This compound features a hydroxypropoxy substituent at the 7-position, contributing to its solubility and potential biological activity. The presence of the hydroxy group enhances its ability to form hydrogen bonds, which may influence its interactions with biological targets. The compound is typically studied for its potential pharmacological properties, including anti-inflammatory and anticancer activities, owing to the structural motifs common in bioactive molecules. Its molecular structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and esterifications. Additionally, the compound's stability, solubility, and reactivity can be influenced by the functional groups present, making it a subject of interest in medicinal chemistry and drug development. As with many quinazolinone derivatives, it may exhibit a range of biological activities, warranting further investigation into its therapeutic potential.

CAS 557770-89-5

7-(3-hydroxypropoxy)quinazolin-4(3H)-one

7-(3-Hydroxy-propoxy)-3H-quinazolin-4-one

Ref: IN-DA00D95R

7-(3-Hydroxypropoxy)quinazolin-4-ol

Ref: 54-OR1002275

7-(3-Hydroxypropoxy)quinazolin-4(3H)-one

Ref: 10-F091794