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Fenamidin

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Identification
Molecular formula
C14H13N3S
CAS number
37932-34-6
IUPAC name
3-anilino-1-phenylimino-isothiourea
State
State

At room temperature, Fenamidin is commonly found in a solid state. The compound is stable under standard conditions but should be handled to avoid prolonged exposure to heat or moisture.

Melting point (Celsius)
198.00
Melting point (Kelvin)
471.00
Boiling point (Celsius)
418.00
Boiling point (Kelvin)
691.00
General information
Molecular weight
256.34g/mol
Molar mass
256.3280g/mol
Density
1.4600g/cm3
Appearence

Fenamidin appears as a crystalline solid that is typically white to off-white in color.

Comment on solubility

Solubility of 3-anilino-1-phenylimino-isothiourea

The solubility of 3-anilino-1-phenylimino-isothiourea (C14H13N3S) is influenced by its unique chemical structure. Here are a few important points regarding its solubility:

  • Solvent Interaction: The presence of both aniline and isothiourea functional groups suggests that this compound may exhibit modest solubility in polar solvents such as water due to the ability to form hydrogen bonds.
  • Organic Solvents: Conversely, it may demonstrate better solubility in non-polar organic solvents, which can effectively solvate the hydrophobic phenyl groups.
  • Temperature Dependency: Increasing the temperature may enhance the solubility in many solvents, a common behavior for many organic compounds, potentially allowing the compound to dissolve more readily.
  • pH Influence: The solubility can also be influenced by the pH of the solution, as protonation of the nitrogen atoms can alter the solvation dynamics.

In summary, the solubility of 3-anilino-1-phenylimino-isothiourea can be characterized by its affinity for both polar and non-polar environments, making it a compound of interest in various chemical and industrial applications.

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.