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2-(Diethylamino)ethyliminomethanedithiol

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Identification
Molecular formula
C7H15N1S2
CAS number
14970-87-7
IUPAC name
2-(diethylamino)ethyliminomethanedithiol
State
State

At room temperature, the compound is typically in a liquid state.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
140.00
Boiling point (Kelvin)
413.15
General information
Molecular weight
177.33g/mol
Molar mass
178.3400g/mol
Density
1.0490g/cm3
Appearence

The compound typically appears as a colorless to pale yellow liquid. Due to its reactive nature, it may darken upon exposure to air.

Comment on solubility

Solubility of 2-(diethylamino)ethyliminomethanedithiol

The solubility characteristics of 2-(diethylamino)ethyliminomethanedithiol present intriguing aspects for consideration. This compound, notable for its complex structure, has several factors affecting its solubility:

  • Polarity: Due to the presence of both polar and nonpolar groups within its structure, 2-(diethylamino)ethyliminomethanedithiol exhibits a moderate level of polarity. This often results in solubility in polar solvents, such as water or ethanol.
  • Hydrogen Bonding: The functional groups capable of forming hydrogen bonds enhance its solubility in alcohols and other protic solvents. The sulfur atoms also contribute to unique solvate interactions.
  • Chain Length: The diethylamino moiety can introduce significant hydrophobic character, which may hinder solubility in highly polar environments but increase compatibility with organic solvents.
  • Temperature Dependency: Like many organic compounds, its solubility may vary with temperature; generally, higher temperatures can facilitate greater solubility.

To sum it up, while 2-(diethylamino)ethyliminomethanedithiol is soluble in certain polar solvents, its overall solubility profile is complex. As a rule of thumb, it is best to evaluate solubility in the intended solvent before practical applications.

Interesting facts

Interesting Facts about 2-(diethylamino)ethyliminomethanedithiol

2-(diethylamino)ethyliminomethanedithiol is a fascinating compound that belongs to a class of substances with unique chemical properties. Here are some enriching aspects of this compound:

  • Functional Group Diversity: This compound features a thioether and an imine functional group, which contribute to its reactivity and versatility in organic synthesis.
  • Applications in Organic Synthesis: The presence of both thio and imino groups makes it an excellent candidate for various synthetic pathways, including the formation of new carbon-sulfur and carbon-nitrogen bonds.
  • Potential Biological Activity: Compounds with similar structures have been studied for their biological activities, including antimicrobial and anticancer properties, making this compound intriguing for pharmaceutical research.
  • Research in Coordination Chemistry: Due to its nitrogen and sulfur donor atoms, it may serve as a ligand in coordination complexes, which are important in catalysis and materials science.
  • Method of Synthesis: The synthesis of this compound often involves multi-step reactions, demonstrating the creativity and problem-solving skills essential in organic chemistry.

As a student or researcher, exploring the characteristics and potential applications of 2-(diethylamino)ethyliminomethanedithiol could lead to exciting discoveries and innovations in both synthetic methods and practical applications.

In summary, this compound is not just another molecule; it embodies the intersection of creativity and utility in the realm of chemistry.