3-(4-aminophenyl)sulfonylisothiourea

Identification

Molecular formula

C₇H₁₀N₂O₂S₂

CAS number

59721-29-8

IUPAC name

3-(4-aminophenyl)sulfonylisothiourea

State

At room temperature, 3-(4-aminophenyl)sulfonylisothiourea usually exists in a solid state. Its stability and form make it suitable for various chemical applications, especially in analytical processing and research.

Melting point (Celsius)

163.00

Melting point (Kelvin)

436.15

Boiling point (Celsius)

435.00

Boiling point (Kelvin)

708.15

General information

Molecular weight

257.30g/mol

Molar mass

257.3250g/mol

Density

1.4500g/cm³

Appearence

3-(4-Aminophenyl)sulfonylisothiourea is typically a crystalline solid. The exact color and texture can vary depending on the purity of the compound, but it is often off-white or pale yellow due to its aromatic and sulfonyl structural components.

Comment on solubility

Solubility of 3-(4-aminophenyl)sulfonylisothiourea

The solubility of 3-(4-aminophenyl)sulfonylisothiourea (C₇H₁₀N₂O₂S₂) can be quite intriguing, especially considering its structural features. Understanding its solubility is essential, and here are some key points to consider:

Solvent Dependency: The solubility of this compound is likely to vary significantly depending on the solvent used. Common solvents to explore include:

Water
Alcohols (like ethanol and methanol)
Dimethyl sulfoxide (DMSO)

Hydrophilicity vs. Hydrophobicity: Given the presence of sulfonyl (–SO₂) and amine (–NH₂) groups, the compound exhibits a tendency toward hydrophilicity, which typically enhances solubility in polar solvents.
Temperature Influence: Like many solutes, temperature plays a crucial role in solubility. Increased temperatures often lead to higher solubility.

In summary, while the solubility profile of 3-(4-aminophenyl)sulfonylisothiourea is influenced by a variety of factors, it is indicative of general trends seen in many amine-containing compounds. As with many substances, it is advisable to conduct empirical testing under specific conditions to confirm solubility behavior.

Interesting facts

Interesting Facts about 3-(4-Aminophenyl)sulfonylisothiourea

3-(4-Aminophenyl)sulfonylisothiourea is a fascinating compound that occupies a unique position in both organic chemistry and medicinal chemistry. Here are some engaging aspects of this compound:

Structure and Function: The compound features both sulfonamide and isothiourea functional groups, which enhance its potential as a bioactive molecule. This unique combination prompts interest for medicinal applications due to potential inhibitory mechanisms.
Biological Relevance: Compounds related to sulfonylureas are known for their role in the treatment of diabetes, functioning by stimulating insulin release from pancreatic beta cells. Although this compound is primarily of interest for its synthetic pathways, it shares structural elements with those medicinally relevant compounds.
Research Application: It can serve as a starting material or intermediate in the synthesis of various pharmaceutical agents. Its ability to modify other chemical structures makes it a valuable compound in drug design and biological research.
Analytical Techniques: The study of 3-(4-aminophenyl)sulfonylisothiourea often involves techniques such as NMR spectroscopy, mass spectrometry, and X-ray crystallography. These tools are crucial for understanding its structural properties and interactions.
Potential Uses: Beyond its current studies, it offers potential for developing new therapeutic agents by altering its substituents, which may yield compounds with novel biological activity.

In conclusion, while 3-(4-aminophenyl)sulfonylisothiourea may not be as widely recognized as some other compounds, its intriguing structure and possible applications in pharmaceutical chemistry make it a noteworthy subject of research. As scientists continue to explore this area, it might reveal even more valuable insights into drug development.