5-Phenyl-1,3-benzoxazole-2-thiol

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Identification

Molecular formula
C13H9NOS
CAS Number
39987-31-8
IUPAC Name
5-phenyl-1,3-benzoxazole-2-thiol
Molecular Weight
227.27g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3225g/cm3
Interesting facts

Interesting Facts about 5-Phenyl-1,3-benzoxazole-2-thiol

5-Phenyl-1,3-benzoxazole-2-thiol is a fascinating compound that belongs to the class of benzoxazoles, which are widely recognized for their diverse biochemical activities and applications. Here are some intriguing aspects of this compound:

  • Biological Activity: This compound exhibits interesting biological properties, including potential antimicrobial and anticancer activities. Research has indicated that derivatives of benzoxazoles can inhibit the growth of various cancer cell lines.
  • Fluorescent Properties: 5-Phenyl-1,3-benzoxazole-2-thiol is known for its ability to fluoresce, making it useful in various chemical and biological assays. Its fluorescent characteristics can be leveraged in microscopy and imaging studies.
  • Design and Synthesis: The synthesis of benzoxazole derivatives involves several methodologies, including condensation reactions and cyclization processes. The presence of the thiol group in this compound enhances its reactivity, allowing further chemical modifications and applications.
  • Applications: This compound plays a role in the development of optical brighteners, dyes, and sensors. Its unique structural features enable its use in designing materials with specific photoluminescent properties.
  • Research Significance: Due to its promising pharmacological properties, 5-phenyl-1,3-benzoxazole-2-thiol has become a subject of significant research interest, opening avenues for drug development and biochemistry.

In summary, the world of 5-phenyl-1,3-benzoxazole-2-thiol is rich with potential, making it an exciting topic for scientists and chemists alike. Its biological activities, fluorescent properties, and diverse applications underscore the importance of exploring such compounds in chemical research.

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