Fenamidin

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Identification

Molecular formula
C14H13N3S
CAS Number
37932-34-6
IUPAC Name
3-anilino-1-phenylimino-isothiourea
Molecular Weight
256.34g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4600g/cm3
Interesting facts

Interesting Facts About 3-anilino-1-phenylimino-isothiourea

3-anilino-1-phenylimino-isothiourea is a fascinating compound that combines elements from both organic and inorganic chemistry in a unique manner. Here are some interesting facts about this compound:

  • Structural Features: This compound features an intriguing isothiourea functional group, which is known for its reactivity and versatility in various chemical processes.
  • Biological Relevance: The aniline and phenyl groups in its structure contribute to its potential biological activities, making it a candidate for various pharmacological studies.
  • Research Applications: Compounds like 3-anilino-1-phenylimino-isothiourea are often explored in fields such as medicinal chemistry due to their potential as drug candidates.
  • Reactivity: Isothioureas are recognized for their ability to undergo nucleophilic substitutions, which can lead to the synthesis of more complex compounds.
  • Analytical Insights: Scientists employ sophisticated techniques like NMR and IR spectroscopy to analyze and confirm the structure of this compound, providing insights into its bonding and functional groups.
  • Potential Uses: These compounds may serve as intermediates in the synthesis of agrochemicals and dyes, reflecting their importance in both agriculture and materials science.

As you study 3-anilino-1-phenylimino-isothiourea, consider the broader implications of its unique structure and reactivity. The intersection of various chemical disciplines opens up numerous possibilities for innovation and application.

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