3-Amino-6-bromoquinazolin-4(3H)-one is a heterocyclic organic compound characterized by its quinazoline core, which consists of a fused benzene and pyrimidine ring. The presence of an amino group at the 3-position and a bromo substituent at the 6-position contributes to its reactivity and potential biological activity. This compound typically exhibits properties such as moderate solubility in polar solvents and may have varying solubility in non-polar solvents, depending on the specific conditions. Its structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The compound may also display properties such as fluorescence or UV absorbance, which can be useful in analytical applications. Additionally, due to the presence of halogen and amino functional groups, it may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Overall, 3-amino-6-bromoquinazolin-4(3H)-one is a versatile compound with potential applications in drug discovery and development.

3-amino-6-bromoquinazolin-4(3H)-one

96498-79-2: 3-Amino-6-bromoquinazolin-4(3H)-one is a heterocyclic organic compound characterized by its quinazoline core, which consists of a fused benzene and pyrimidine ring. The presence of an amino group at the 3-position and a bromo substituent at the 6-position contributes to its reactivity and potential biological activity. This compound typically exhibits properties such as moderate solubility in polar solvents and may have varying solubility in non-polar solvents, depending on the specific conditions. Its structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The compound may also display properties such as fluorescence or UV absorbance, which can be useful in analytical applications. Additionally, due to the presence of halogen and amino functional groups, it may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Overall, 3-amino-6-bromoquinazolin-4(3H)-one is a versatile compound with potential applications in drug discovery and development.

CAS 96498-79-2

3-amino-6-bromoquinazolin-4(3H)-one

3-Amino-6-bromo-3,4-dihydroquinazolin-4-one

Ref: 3D-WDA49879