Fenobucarb

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Identification

Molecular formula
C15H14N2O2S
CAS Number
3767-28-0
IUPAC Name
1-(6-methoxy-1,3-benzothiazol-2-yl)-3-phenyl-urea
Molecular Weight
225.28g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3400g/cm3
Appearance
can vary slightly depending on the specific impurities and the processing methods used.
Synonyms
FRENTIZOLE
Interesting facts

Interesting Facts about 1-(6-methoxy-1,3-benzothiazol-2-yl)-3-phenyl-urea

1-(6-methoxy-1,3-benzothiazol-2-yl)-3-phenyl-urea is an intriguing compound with a variety of applications and properties that make it a subject of interest among chemists and pharmacologists alike. Here are some key points about this fascinating molecule:

  • Structure and Design: This compound features a unique combination of a urea moiety and a benzothiazole ring, which contributes to its biological activity. The design allows for multiple interactions within biological systems, making it an excellent candidate for drug development.
  • Biological Activity: Compounds like this one often exhibit promising pharmacological properties. Research indicates that benzothiazole derivatives may possess antitumor, antibacterial, and anti-inflammatory effects, suggesting potential roles in therapeutic applications.
  • Mechanism of Action: The presence of the methoxy group can enhance the lipophilicity and stability of the compound, which is crucial for its interaction with target sites in biological systems. This modification can influence the pharmacodynamics significantly.
  • Versatile Applications: Due to its biological properties, this compound could be explored in various fields including medicinal chemistry, agriculture (as a plant growth regulator), and material sciences for developing advanced materials.
  • Research Potential: The ongoing exploration of similar derivatives continues to reveal new pathways for synthesis and application. This compound could serve as a lead structure for synthesizing new, more effective therapeutic agents.

In summary, 1-(6-methoxy-1,3-benzothiazol-2-yl)-3-phenyl-urea stands as a testament to the creativity and innovation in chemistry. As the field evolves, it will be exciting to uncover new uses and understand the mechanisms driving its biological activities.

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