6-Bromo-2(3H)-benzoxazolone

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Identification

Molecular formula
C7H4BrNO2
CAS Number
635-21-2
IUPAC Name
6-bromo-3H-1,3-benzoxazol-2-one
Molecular Weight
212.02g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
and crystalline nature.
Synonyms
6-bromobenzo[d]oxazol-2(3H)-one
Interesting facts

Interesting Facts about 6-bromo-3H-1,3-benzoxazol-2-one

6-bromo-3H-1,3-benzoxazol-2-one, often abbreviated for convenience, is a fascinating compound that belongs to the class of substituted benzoxazoles. Here are some engaging insights about this intriguing chemical:

  • Structure and Function: The compound contains a benzoxazole ring, which offers significant aromatic stabilization. This structure is crucial for its biological activity and interactions.
  • Applications: 6-bromo-3H-1,3-benzoxazol-2-one is often used in the development of pharmaceuticals and agrochemicals. Its derivatives have been studied for their potential as antimicrobial and antitCancer agents, thereby showcasing its importance in medicinal chemistry.
  • Research Significance: Researchers have found that compounds like 6-bromo-3H-1,3-benzoxazol-2-one can serve as vital tools in the study of various biochemical pathways. They can act as enzyme inhibitors or modulators, providing deeper insights into complex biological mechanisms.
  • Functional Group Chemistry: The presence of the bromo substituent enhances its reactivity, allowing for further functionalization. This makes it a versatile building block in organic synthesis.
  • Tutorials and Experiments: In an academic setting, students often explore this compound in the context of reaction mechanisms and synthetic pathways, allowing them to grasp fundamental concepts in organic and medicinal chemistry.

In summary, 6-bromo-3H-1,3-benzoxazol-2-one is not just another chemical compound. Its unique structure and diverse applications make it a subject of ongoing research and interest within the scientific community. As we expand our understanding of compounds like this, we take important strides in drug discovery and development.

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