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.
Synonyms
          6-bromobenzo[d]oxazol-2(3H)-one
          6-bromo-2(3H)-benzoxazolone
          6-bromo-2,3-dihydro-1,3-benzoxazol-2-one
          6-bromobenzo(d)oxazol-2(3H)-one
          626-327-4
          947-686-6
          RefChem:540616
          19932-85-5
          6-Bromo-2-benzoxazolinone
          2(3H)-Benzoxazolone, 6-bromo-
          6-bromo-1,3-benzoxazol-2(3H)-one
          Cincreasin
          6-bromo-3H-1,3-benzoxazol-2-one
          6-Bromobenzoxazolinone
          6-Bromo-benzoxazolinone
          2-BENZOXAZOLINONE, 6-BROMO-
          MFCD00694727
          6-Bromobenzoxazol-2(3H)-one
          6-bromo-3H-benzoxazol-2-one
          MLS002639099
          6-Bromo-3H-benzooxazol-2-one
          CHEBI:77861
          NSC-26190
          BRN 0135506
          6-Bromobenzoksazolinon-2 [Polish]
          6-Bromobenzoksazolinon-2
          NSC 26190
          NSC26190
          6-bromobenzoxazolone
          6-bromo benzoxazolinone
          6-Bromo-2-benzoxazolone
          2QUP5AFH6S
          6-Bromo-2-hydroxybenzoxazole
          SCHEMBL1762301
          6-bromo-1,3-benzoxazol-2-ol
          CHEMBL1898381
          SCHEMBL31334714
          6-bromo-3-hydrobenzoxazol-2-one
          DTXSID70173710
          6-Bromo-2-benzoxazolinone, 97%
          HMS3080E07
          BCP26435
          SBB094871
          STK802473
          STL273089
          AKOS003388134
          AKOS016402889
          CS-W022467
          HD-0708
          AC-30754
          BP-20118
          SMR001548550
          SY038492
          DB-029220
          B5290
          EN300-37479
          Q27147469
          Z381351238
              
Solubility of 6-bromo-3H-1,3-benzoxazol-2-one
The solubility of 6-bromo-3H-1,3-benzoxazol-2-one can be characterized by its behavior in various solvents. As with many organic compounds, its solubility depends on several factors, including:
For 6-bromo-3H-1,3-benzoxazol-2-one, its structure suggests some degree of polarity due to the presence of bromine and the benzoxazole moiety. This compound typically exhibits:
In summary: The solubility of 6-bromo-3H-1,3-benzoxazol-2-one is influenced by solvent choice, temperature, and pH. Experimentation with various conditions can yield optimal solubility characteristics for practical applications.