6-Bromo-4-methoxy-quinazoline is a heterocyclic organic compound characterized by its quinazoline core, which consists of a fused benzene and pyrimidine ring. The presence of a bromine atom at the 6-position and a methoxy group at the 4-position 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 characteristics. The bromine substituent can enhance the compound's reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The methoxy group can influence the electronic properties of the molecule, potentially affecting its biological activity. Compounds of this class are often studied for their pharmacological properties, including potential anti-cancer and anti-inflammatory activities. As with many heterocycles, the specific interactions and reactivity of 6-bromo-4-methoxy-quinazoline can be influenced by the presence of functional groups and the overall molecular structure, making it a subject of interest in medicinal chemistry and drug development.

6-bromo-4-methoxy-quinazoline

915924-79-7: 6-Bromo-4-methoxy-quinazoline is a heterocyclic organic compound characterized by its quinazoline core, which consists of a fused benzene and pyrimidine ring. The presence of a bromine atom at the 6-position and a methoxy group at the 4-position 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 characteristics. The bromine substituent can enhance the compound's reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The methoxy group can influence the electronic properties of the molecule, potentially affecting its biological activity. Compounds of this class are often studied for their pharmacological properties, including potential anti-cancer and anti-inflammatory activities. As with many heterocycles, the specific interactions and reactivity of 6-bromo-4-methoxy-quinazoline can be influenced by the presence of functional groups and the overall molecular structure, making it a subject of interest in medicinal chemistry and drug development.

CAS 915924-79-7

6-bromo-4-methoxy-quinazoline

6-Bromo-4-methoxyquinazoline

Ref: IN-DA00GTRD

6-Bromo-4-methoxyquinazoline

Ref: 54-OR1066971

6-bromo-4-methoxyquinazoline

Ref: 10-F309402