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3-(1-phenylethylideneamino)isothiourea

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Identification
Molecular formula
C9H12N2S
CAS number
26369-66-0
IUPAC name
3-(1-phenylethylideneamino)isothiourea
State
State

At room temperature, 3-(1-phenylethylideneamino)isothiourea is typically a solid. It is often described as having a crystalline powder form.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
330.20
Boiling point (Kelvin)
603.35
General information
Molecular weight
179.27g/mol
Molar mass
179.2700g/mol
Density
1.2400g/cm3
Appearence

This compound typically appears as a white to light yellow crystalline powder. The color intensity can vary slightly depending on the specific synthesis and purity.

Comment on solubility

Solubility of 3-(1-phenylethylideneamino)isothiourea

3-(1-phenylethylideneamino)isothiourea, known for its unique structure, presents interesting solubility characteristics:

  • Polarity Considerations: The presence of both hydrophilic (amino) and hydrophobic (phenyl) groups can lead to varied solubility behaviors.
  • Solvent Compatibility: Generally, compounds like this are expected to have better solubility in polar solvents like water and ethanol, while being less soluble in non-polar solvents like hexane.
  • Temperature Effects: Solubility can be influenced by temperature; typically, higher temperatures result in increased solubility for most organic compounds.

As stated, "Solubility is a key factor that dictates the behavior of chemical compounds in various environments." Understanding the solubility of 3-(1-phenylethylideneamino)isothiourea is essential for applications in pharmaceuticals and materials science. Its unique balance of polar and non-polar features plays a significant role in its solubility profile, making it a fascinating compound in the realm of chemical research.

Interesting facts

Interesting Facts about 3-(1-phenylethylideneamino)isothiourea

3-(1-phenylethylideneamino)isothiourea is a fascinating organic compound, attracting attention for its unique structure and potential applications in various scientific fields. Below are some key points highlighting its significance:

  • Diverse Applications: This compound is often explored in the realm of medicinal chemistry, where its derivatives may exhibit biological activity. Researchers are particularly interested in its potential use as a therapeutic agent.
  • Structural Features: The isothiourea moiety is of particular interest because compounds containing this functional group have been associated with a variety of biological properties, including anti-inflammatory and antimicrobial activities.
  • Research Interest: Studies are underway to understand the reactivity of 3-(1-phenylethylideneamino)isothiourea and how modifications to its structure can enhance its efficacy and selectivity in biological systems.
  • Synthesis: The synthetic pathways leading to the formation of this compound often involve the reaction of isothiocyanates with amines, showcasing fundamental organic reactions that are crucial in both educational and research settings.

In summary, 3-(1-phenylethylideneamino)isothiourea represents a blend of organic chemistry and medicinal science, encouraging scientists to explore its potential benefits further. As research unfolds, this compound may reveal unknown properties that could lead to innovative applications.