8-Bromoquinazoline is a heterocyclic organic compound characterized by the presence of a bromine atom at the 8-position of the quinazoline ring system. Quinazoline itself is a bicyclic structure composed of a benzene ring fused to a pyrimidine ring, which contributes to its aromatic properties. The introduction of the bromine substituent enhances its reactivity and can influence its biological activity, making it of interest in medicinal chemistry. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water, which is common for many halogenated heterocycles. Its molecular structure allows for potential interactions with various biological targets, and it may serve as a scaffold for the development of pharmaceuticals, particularly in the fields of oncology and neurology. Additionally, 8-bromoquinazoline can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. As with many brominated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns.

8-bromoquinazoline

1123169-41-4: 8-Bromoquinazoline is a heterocyclic organic compound characterized by the presence of a bromine atom at the 8-position of the quinazoline ring system. Quinazoline itself is a bicyclic structure composed of a benzene ring fused to a pyrimidine ring, which contributes to its aromatic properties. The introduction of the bromine substituent enhances its reactivity and can influence its biological activity, making it of interest in medicinal chemistry. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water, which is common for many halogenated heterocycles. Its molecular structure allows for potential interactions with various biological targets, and it may serve as a scaffold for the development of pharmaceuticals, particularly in the fields of oncology and neurology. Additionally, 8-bromoquinazoline can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. As with many brominated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns.

CAS 1123169-41-4

8-bromoquinazoline

8-Bromoquinazoline

Ref: IN-DA007BFZ

8-Bromoquinazoline

Ref: 54-OR94472

8-Bromoquinazoline

Ref: 10-F225135

8-Bromoquinazoline

Ref: 3D-YUB16941