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4-(1,3,2-dithiarsolan-2-yl)-N,N-diethyl-aniline

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Identification
Molecular formula
C12H18AsNS2
CAS number
235823-51-7
IUPAC name
4-(1,3,2-dithiarsolan-2-yl)-N,N-diethyl-aniline
State
State

Solid at room temperature. It holds a crystalline structure.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
297.48g/mol
Molar mass
297.4780g/mol
Density
1.3400g/cm3
Appearence

The compound is typically a solid at room temperature with a pale yellow or off-white color. It is crystalline in nature and may have a characteristic odor associated with its aromatic and diethylamine components.

Comment on solubility

Solubility of 4-(1,3,2-dithiarsolan-2-yl)-N,N-diethyl-aniline

The solubility of the compound 4-(1,3,2-dithiarsolan-2-yl)-N,N-diethyl-aniline is influenced by its unique structural characteristics, primarily its polar and non-polar regions. Here are some key aspects to consider:

  • Polarity: The presence of the dithiarsolane group introduces polar characteristics, which may enhance solubility in polar solvents, such as water and alcohols.
  • Non-polar Regions: The diethyl group contributes to non-polar characteristics, which can limit solubility in highly polar solvents but improve solubility in organic solvents.
  • Solvent Dependency: The compound is expected to display varying solubility depending on the solvent used:
    • More soluble in polar organic solvents
    • Less soluble in non-polar solvents
  • Temperature Effects: Solubility can also be temperature-dependent, and as temperature increases, the solubility of many compounds generally increases due to enhanced molecular motion.

In conclusion, while specific solubility data may be limited, 4-(1,3,2-dithiarsolan-2-yl)-N,N-diethyl-aniline is likely to exhibit complex solubility behavior that makes it more suited for certain solvents over others. Understanding these characteristics is crucial for practical applications.

Interesting facts

Interesting Facts About 4-(1,3,2-Dithiarsolan-2-yl)-N,N-diethyl-aniline

The compound 4-(1,3,2-dithiarsolan-2-yl)-N,N-diethyl-aniline is a fascinating example of a hybrid organic compound that incorporates both nitrogen and sulfur elements. Here are some intriguing aspects of this compound:

  • Organosulfur Chemistry: This compound is significant in the field of organosulfur chemistry, which explores the chemistry of sulfur-containing compounds. Such compounds are known for their diverse applications in pharmaceuticals and agrochemicals.
  • Structural Complexity: Featuring both a dithiarsolan ring and a diethyl-aniline structure, it exemplifies structural complexity and offers various sites for chemical reactivity, making it an important subject of study in synthetic organic chemistry.
  • Potential Biological Activity: Given the presence of the dithiarsolan moiety, compounds like this may exhibit interesting biological activities, including antioxidant properties or potential applications in drug development.
  • Environmental Impact: The incorporation of sulfur in chemicals has implications for environmental chemistry. Understanding such compounds contributes to the evaluation of their environmental impact and persistence.
  • Synthetic Routes: The synthesis of this compound may involve various organic reactions such as nucleophilic substitution or electrophilic aromatic substitution, providing insight into practical methodologies in organic synthesis.
  • Research Interest: Researchers investigate compounds like this not just for their potential applications but also as models to understand the reactivity and properties of similar sulfur-containing systems.

Understanding compounds such as 4-(1,3,2-dithiarsolan-2-yl)-N,N-diethyl-aniline enriches our knowledge of chemical diversity and functionalization, demonstrating the versatility of sulfur in organic chemistry.

As the famous chemist Linus Pauling once said, "The world will never be the same again after the discovery of the structure of DNA." Similarly, the exploration of complex compounds like this can pave the way for new scientific breakthroughs in medicinal chemistry and material science!

Synonyms
5185-78-4
BRN 2848789
2-(p-Diethylaminophenyl)-1,3,2-dithiarsenolane
1,3,2-DITHIARSENOLANE, 2-(p-(DIETHYLAMINO)PHENYL)-
DTXSID60199808
DTXCID80122299