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1,3-Dianilinoisothiourea

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Identification
Molecular formula
C13H14N4S
CAS number
102517-75-1
IUPAC name
1,3-dianilinoisothiourea
State
State

At room temperature, 1,3-Dianilinoisothiourea is a crystalline solid. It is typically stable in ambient conditions but should be handled with care to prevent exposure to moisture and air, which may cause degradation.

Melting point (Celsius)
192.00
Melting point (Kelvin)
465.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
277.36g/mol
Molar mass
277.3600g/mol
Density
1.4000g/cm3
Appearence

1,3-Dianilinoisothiourea is typically a solid compound that appears as a crystalline powder. Its color can range from white to light yellow. The substance may have a faint aromatic odor due to the aniline groups in its structure.

Comment on solubility

Solubility of 1,3-Dianilinoisothiourea

1,3-Dianilinoisothiourea, with its intriguing structure, presents interesting solubility characteristics. Understanding its solubility profile is essential for various applications in chemistry and biochemistry.

General Solubility Behavior

When examining the solubility of 1,3-dianilinoisothiourea, consider the following points:

  • Polar Organic Solvents: The compound generally demonstrates solubility in various polar organic solvents, influenced by the presence of the thiourea functional group.
  • Water Solubility: Its solubility in water is limited, indicating it is not highly soluble in polar environments.
  • pH Dependency: The solubility can vary with pH levels, potentially increasing in acidic conditions where protonation may occur.

Factors Influencing Solubility

The solubility characteristics of 1,3-dianilinoisothiourea can be attributed to several factors:

  • Molecular Structure: The arrangement of aromatic groups can affect how well the compound interacts with solvents.
  • Temperature: Increasing temperature may enhance solubility in organic solvents.
  • Concentration of Solutions: Higher concentrations could lead to significant changes in solubility due to intermolecular interactions.

Overall, while 1,3-dianilinoisothiourea shows promise for solubility in specific solvents, its limited solubility in water may restrict its use in aqueous environments. The delicate balance of factors influencing its solubility makes it a fascinating compound worthy of exploration.

Interesting facts

Interesting Facts about 1,3-Dianilinoisothiourea

1,3-Dianilinoisothiourea is a fascinating compound that is part of the family of thioureas, which are known for their intriguing chemical properties and applications. Here are some notable aspects of this compound:

  • Versatile Applications: This compound has been studied for its potential applications in various fields such as agriculture, pharmaceuticals, and material science. Its ability to act as a fungicide and herbicide makes it quite valuable in agricultural chemistry.
  • Biological Activity: Like many thioureas, 1,3-dianilinoisothiourea has been observed to exhibit biological activity, including anti-cancer properties. Researchers are particularly interested in its mechanism of action against tumor cells.
  • Synthesis Pathway: The synthesis typically involves the reaction of diarylamines with isothiocyanates, a reaction that is both straightforward and efficient, fostering research into novel thiourea derivatives.
  • Research Tool: In chemical research, compounds like 1,3-dianilinoisothiourea serve as valuable tools for studying the properties of various chemical reactions and mechanisms, enhancing our understanding of thiourea chemistry.
  • Significance in Coordination Chemistry: This compound has been explored for its role in coordination chemistry, where it can act as a ligand, forming complexes that might have useful properties.

In summary, 1,3-dianilinoisothiourea is an intriguing compound that presents a plethora of opportunities for further exploration and application. As researchers delve deeper into its properties, we may uncover even more exciting uses that can impact various scientific disciplines.