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1,3-Bis(ethylsulfanylmethyl)imidazolidinium dichloride

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Identification
Molecular formula
C11H24Cl2N2S2
CAS number
23860-41-7
IUPAC name
1,3-bis(ethylsulfanylmethyl)imidazolidine-1,3-diium;dichloride
State
State

This compound is typically found in a solid state at room temperature.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.00
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.00
General information
Molecular weight
298.28g/mol
Molar mass
298.2800g/mol
Density
1.3000g/cm3
Appearence

The compound typically appears as a white or off-white crystalline solid.

Comment on solubility

Solubility of 1,3-bis(ethylsulfanylmethyl)imidazolidine-1,3-diium; dichloride

The solubility of 1,3-bis(ethylsulfanylmethyl)imidazolidine-1,3-diium; dichloride can be analyzed through several important factors that determine its behavior in various solvents.

Factors Influencing Solubility

  • Polarity: This compound contains several polar functional groups, suggesting that it may have decent solubility in polar solvents such as water.
  • Hydrogen Bonding: The imidazolidine structure enables the potential for hydrogen bonding, which can further enhance solubility in polar media.
  • Electrolytic Behavior: Given that it contains chloride ions, the compound is likely to disassociate in solution, affecting its overall solubility dynamics.

In general, ionic compounds tend to be more soluble in polar solvents, while organic compounds exhibit varied solubility based on their functional groups. It’s essential to also consider concentration effects, temperature, and the presence of other ions or solutes in the solution, which can either promote or hinder solubility. As a specific example, it has been noted that:

"The solubility behavior of complex organic salts is often a balance between ionic dissolution and molecular interactions."

In summary, 1,3-bis(ethylsulfanylmethyl)imidazolidine-1,3-diium; dichloride is expected to demonstrate reasonable solubility in polar solvents, driven by its ionic character and polar functional groups. Further experimental data would provide a clearer understanding of its solubility profile in various conditions.

Interesting facts

Interesting Facts about 1,3-bis(ethylsulfanylmethyl)imidazolidine-1,3-diium;dichloride

The compound known as 1,3-bis(ethylsulfanylmethyl)imidazolidine-1,3-diium;dichloride is a fascinating member of the imidazolidine family. Here are some intriguing insights into this chemical:

  • Dual Functionality: This compound serves as both a reducing agent and a stabilizing agent. Its unique structure allows it to participate in various chemical reactions, often leading to the formation of more complex molecules.
  • Biological Implications: The presence of sulfur in the compound can play a significant role in biological systems, influencing enzyme activities and metabolic processes. Sulfur-containing compounds are often involved in redox (reduction-oxidation) reactions that are central to life.
  • Polyvalent Nature: The imidazolidine scaffold provides a environment that can attract different types of functional groups, making this compound a versatile building block in synthetic chemistry.
  • Applications in Organic Synthesis: The compound is utilized in the synthesis of various pharmaceutical agents and agrochemicals due to its favorable chemical properties.
  • Structure-Activity Relationship: Understanding how the arrangement of atoms in 1,3-bis(ethylsulfanylmethyl)imidazolidine-1,3-diium affects its reactivity and interaction with other molecules is crucial for chemists. Such studies can lead to the design of more effective compounds in the field of medicinal chemistry.

In summary, 1,3-bis(ethylsulfanylmethyl)imidazolidine-1,3-diium;dichloride showcases the importance of chemical structure in determining reactivity, biological activity, and potential applications in various fields. As research continues, the full potential of this compound is yet to be uncovered!

Synonyms
1,3-Diethylthiomethylimidazolidine dihydrochloride
4082-71-7
1,3-Diaethylthiomethyl-imidazolidin-dihydrochlorid [German]
IMIDAZOLIDINE, 1,3-DIETHYLTHIOMETHYL-, DIHYDROCHLORIDE
1,3-Diaethylthiomethyl-imidazolidin-dihydrochlorid