5-Bromoquinoxaline is a heterocyclic compound characterized by its fused benzene and pyridine rings, with a bromine atom substituted at the 5-position of the quinoxaline structure. It has a molecular formula that reflects its composition of carbon, hydrogen, nitrogen, and bromine. This compound is typically a yellow to brown solid and is known for its role in various chemical reactions and applications, particularly in medicinal chemistry and as a building block in the synthesis of other organic compounds. 5-Bromoquinoxaline exhibits biological activity, making it of interest in pharmacological research, particularly for its potential as an antimicrobial or anticancer agent. Its reactivity is influenced by the presence of the bromine atom, which can participate in nucleophilic substitution reactions. Additionally, the compound's solubility varies depending on the solvent, and it may exhibit fluorescence properties, which can be useful in analytical applications. Overall, 5-Bromoquinoxaline is a versatile compound with significant implications in both synthetic and medicinal chemistry.

5-Bromoquinoxaline

Quinoxalines are a class of compounds that have been extensively studied for their photophysical properties. 5-Bromoquinoxaline is one such compound and has been shown to be differentiable from other quinoxalines in its electronic spectra, insensitivity to oxygen, and photophysical properties. The experimental data obtained on 5-bromoquinoxaline has been verified with theoretical calculations. The nature of the substituent attached to the aromatic ring influences the electronic structures and luminescence of this molecule.

CAS 76982-23-5: 5-Bromoquinoxaline

5-Bromoquinoxaline

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5-Bromoquinoxaline

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5-Bromoquinoxaline

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5-Bromoquinoxaline

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