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2-(Dimethylamino)ethanimidothioic acid

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Identification
Molecular formula
C4H10N2OS
CAS number
10414-14-5
IUPAC name
2-(dimethylamino)ethanimidothioic acid
State
State

At room temperature, 2-(Dimethylamino)ethanimidothioic acid is typically a solid.

Melting point (Celsius)
85.00
Melting point (Kelvin)
358.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
118.19g/mol
Molar mass
118.1890g/mol
Density
1.0000g/cm3
Appearence

2-(Dimethylamino)ethanimidothioic acid is generally seen as a colorless to pale yellow crystalline solid. The compound is typically encountered in its synthesized form and can have a slightly pungent odor.

Comment on solubility

Solubility of 2-(dimethylamino)ethanimidothioic acid

2-(dimethylamino)ethanimidothioic acid, a compound featuring a thioamide functional group, presents interesting solubility characteristics. Given its molecular composition, this compound exhibits varied solubility depending on the solvent used.

  • Water Solubility: The presence of both the amino and thio groups suggests some degree of polarity, typically enhancing solubility in polar solvents like water, though empirical data should be consulted for specific solubility values.
  • Organic Solvents: This compound may show improved solubility in organic solvents such as methanol or ethanol, largely due to the hydrophobic character of the dimethylamino group.
  • dilute acids or bases: Solubility may also be influenced by pH, as ionization can enhance solubility in acidic or basic solutions.

In general, solubility can be viewed through the lens of the “like dissolves like” principle, where the polarity of the solvent must align with that of the solute. Thus, the solubility of 2-(dimethylamino)ethanimidothioic acid is a function of its structure and the chemical environment, making it crucial to consider specific conditions during experimentation.

Interesting facts

Interesting Facts about 2-(Dimethylamino)ethanimidothioic Acid

2-(Dimethylamino)ethanimidothioic acid, often abbreviated as DMETAC, is a fascinating compound with notable applications in both the pharmaceutical and chemical industries. Here are some compelling facts about this versatile compound:

  • Biological Activity: DMETAC has shown potential as a biologically active molecule, particularly in medicinal chemistry. Its structure allows for interactions with various biological targets, making it a candidate for further research in drug development.
  • Synthesis: The synthesis of 2-(dimethylamino)ethanimidothioic acid involves unique chemical reactions that utilize aminothio acids, illustrating the compound's complex organic chemistry. This synthetic pathway can be an excellent example for students studying organic synthesis techniques.
  • Applications: Beyond its pharmaceutical implications, DMETAC can also be employed in the field of agrochemicals. *Its ability to function as a thiol-based compound means it could play a role in developing agricultural products.*
  • Structure and Properties: Containing both amine and thiol functional groups, DMETAC exhibits intriguing properties that can be explored in studies on molecular interactions and bonding. The presence of the dimethylamino group also adds to its nucleophilicity, making it an interesting topic for research on reactivity.
  • Research Potential: There is a significant opportunity for future research surrounding DMETAC, particularly in exploring its efficacy and mechanisms of action within biological systems. Scientific inquiry into thiol-containing compounds continues to expand, highlighting the relevance of such compounds in contemporary chemistry.

In summary, 2-(dimethylamino)ethanimidothioic acid is not just a compound of theoretical interest; it offers numerous practical applications and research avenues that can contribute significantly to both scientific understanding and commercial utility.