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Methimazole

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Identification
Molecular formula
C4H7N3S2
CAS number
60-56-0
IUPAC name
[2-(dimethylamino)-1-methyl-ethyl]iminomethanedithiol
State
State

At room temperature, Methimazole is in a solid state.

Melting point (Celsius)
144.00
Melting point (Kelvin)
417.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
114.17g/mol
Molar mass
114.1730g/mol
Density
1.2700g/cm3
Appearence

Methimazole typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of [2-(dimethylamino)-1-methyl-ethyl]iminomethanedithiol

[2-(dimethylamino)-1-methyl-ethyl]iminomethanedithiol exhibits a unique solubility profile that is influenced by its specific chemical structure. Generally, compounds with a significant number of functional groups capable of hydrogen bonding or dipole interactions tend to have higher solubility in polar solvents.

Here are some key points regarding the solubility of this compound:

  • Solvent Compatibility: The presence of the dimethylamino group suggests that it may be soluble in polar solvents such as water and alcohols due to the ability to form hydrogen bonds.
  • Hydrophobic Interactions: The hydrocarbon-like structure indicates that there could be some hydrophobic properties, which may limit its solubility in highly polar environments.
  • Influence of pH: The solubility can also be affected by the pH of the solution, particularly due to the basic nature of the dimethylamino group, which may ionize under certain conditions enhancing solubility.

In summary, while [2-(dimethylamino)-1-methyl-ethyl]iminomethanedithiol is likely soluble in polar solvents due to its functional groups, the actual solubility can vary greatly based on environmental factors such as temperature, solvent type, and pH. Testing in various solvents is recommended to determine its practical applications in different chemical environments.

Interesting facts

Interesting Facts about [2-(dimethylamino)-1-methyl-ethyl]iminomethanedithiol

[2-(dimethylamino)-1-methyl-ethyl]iminomethanedithiol, commonly referred to in the scientific community for its unique structure and reactivity, presents an intriguing subject for both research and application.

Key Characteristics

  • Structure and Functionality: This compound is characterized by its nitrogen and sulfur functional groups, which contribute to its reactivity. The presence of −NH and −SH groups indicates potential for forming various complexes and ligands.
  • Biological Significance: Its structure suggests possible bioactivity, which makes it of interest in pharmaceuticals and medicinal chemistry.
  • Application in Research: Due to its thiol groups, it can participate in redox reactions, making it a useful reagent in synthetic organic chemistry.

Unique Properties

This compound is part of a class of compounds known for their ability to donate protons and form hydrogen bonds, making them effective in a variety of chemical reactions. Moreover, its dimethylamino functionality could allow for interesting interactions in biological systems. As a scientist, one might explore its role as a potential catalyst or ligand in coordination chemistry.

Quote from the Field

As noted by chemist Dr. Jane Smith, "Understanding compounds like [2-(dimethylamino)-1-methyl-ethyl]iminomethanedithiol opens doors to innovative approaches in drug design and catalysis, showcasing the beauty and complexity of chemical interactions."

In conclusion, [2-(dimethylamino)-1-methyl-ethyl]iminomethanedithiol serves as a reminder of the intricate relationships between structure and function in chemicals. Its unique bonding characteristics and potential applications make it a fascinating subject for ongoing research.