5-Chloro-3H-1,3-benzoxazol-2-one
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- Molecular formula
- C7H4ClNO2
- CAS Number
- 135-88-6
- IUPAC Name
- 5-chloro-3H-1,3-benzoxazol-2-one
- Molecular Weight
- 169.57g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5400g/cm3
- Synonyms
- chlorzoxazone
Identification
Interesting facts
Interesting Facts about 5-chloro-3H-1,3-benzoxazol-2-one
5-chloro-3H-1,3-benzoxazol-2-one is a fascinating compound with unique properties and applications that pique the interest of both chemists and biologists. Here are some noteworthy aspects of this compound:
- Structural Features: The compound features a benzoxazole ring, which is notable for its aromatic characteristics and flexibility in forming hydrogen bonds. This ring structure gives rise to interesting reactivity patterns.
- Biological Relevance: Compounds like 5-chloro-3H-1,3-benzoxazol-2-one are often studied for their biological activity. They can exhibit antimicrobial or anti-inflammatory properties, making them subjects of interest in medicinal chemistry.
- Photochemical Applications: Due to its distinct chromophore, this compound can be utilized in photochemical reactions, which are essential in developing new materials and light-activated compounds.
- Synthesis Versatility: The synthesis of benzoxazole derivatives can be achieved through various methods, including cyclization reactions and condensation processes, providing synthetic chemists with flexibility in laboratory settings.
- Research Potential: As a member of the benzoxazole class, 5-chloro-3H-1,3-benzoxazol-2-one opens doors for further research into its derivatives, which could lead to discovering novel agents for pharmaceuticals and agrochemicals.
In summary, 5-chloro-3H-1,3-benzoxazol-2-one is not just a simple chemical compound; it is a promising structure in the field of chemical and biological research that may lead to exciting innovations. The exploration of its properties and applications continues to be a valuable endeavor for scientists worldwide.