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1,3-bis(p-tolyl)isothiourea

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Identification
Molecular formula
C15H16N2S
CAS number
729-14-0
IUPAC name
1,3-bis(p-tolyl)isothiourea
State
State

At room temperature, 1,3-bis(p-tolyl)isothiourea is typically found as a solid.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
485.00
Boiling point (Kelvin)
758.15
General information
Molecular weight
256.37g/mol
Molar mass
256.3560g/mol
Density
1.2350g/cm3
Appearence

1,3-bis(p-tolyl)isothiourea typically appears as a white to off-white crystalline powder. It is often used in research settings where observations about its color and form can be significant when confirming purity or identity of the compound.

Comment on solubility

Solubility of 1,3-bis(p-tolyl)isothiourea

The solubility of 1,3-bis(p-tolyl)isothiourea can be described as rather limited when considering its behavior in various solvents. Here are some key points regarding its solubility:

  • Solvent Interaction: This compound tends to show varying degrees of solubility in organic solvents, reflecting its relatively non-polar characteristics due to the presence of the p-tolyl groups.
  • Aqueous Solubility: In water, the solubility is poor, primarily due to the large size of the organic substituents which restrict the formation of hydrogen bonds with water.
  • Potential Solvent Choices: Common organic solvents such as ethanol and acetone may slightly improve solubility; however, they are not highly soluble.

In summary, 1,3-bis(p-tolyl)isothiourea exhibits limited solubility, particularly in polar solvents like water, but may dissolve to some extent in non-polar or slightly polar organic solvents. Understanding the solubility behaviors helps in processing and utilizing this compound in various chemical applications.

Interesting facts

Interesting Facts about 1,3-bis(p-tolyl)isothiourea

1,3-bis(p-tolyl)isothiourea is a fascinating compound with intriguing properties and applications. This compound belongs to the class of isothioureas, which are organosulfur compounds notable for their versatility in chemistry. Here are some engaging facts about this compound:

  • Versatile Reactivity: Isothioureas, including 1,3-bis(p-tolyl)isothiourea, are known for their ability to participate in a wide variety of chemical reactions. They can act as nucleophiles and can undergo different transformations, making them valuable intermediates in organic synthesis.
  • Biological Activity: Compounds like 1,3-bis(p-tolyl)isothiourea have been studied for their biological activities. Some derivatives exhibit interesting antifungal and antiparasitic properties, and researchers are exploring their potential in medicinal chemistry.
  • Ligand Formation: This compound can form stable complexes with metals, which enables its utilization in coordination chemistry. The interactions with metal ions can lead to new catalytic systems and materials with unique properties.
  • Synthetic Utility: The preparation of 1,3-bis(p-tolyl)isothiourea can be achieved through various synthetic routes, often involving easily accessible starting materials. This makes it an attractive choice for chemists seeking to create complex molecular architectures.
  • Research Interest: Due to its diverse chemical behavior, 1,3-bis(p-tolyl)isothiourea is often a topic of research in fields ranging from organic chemistry to biochemistry. New applications and methodologies are continuously being discovered, highlighting the enduring relevance of this compound.

In conclusion, 1,3-bis(p-tolyl)isothiourea exemplifies the intersection of reactivity, biological importance, and synthetic versatility. As the field of chemistry continues to evolve, this compound remains a compelling subject for exploration.