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4,5-Dihydroimidazole-2-thiol

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Identification
Molecular formula
C3H6N2S
CAS number
551-90-6
IUPAC name
4,5-dihydro-1H-imidazole-2-thiol
State
State

At room temperature, 4,5-Dihydroimidazole-2-thiol is in a solid state.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
104.16g/mol
Molar mass
104.1550g/mol
Density
1.2421g/cm3
Appearence

4,5-Dihydroimidazole-2-thiol typically appears as a crystalline solid, which may be colorless to pale yellow. It has a distinct sulfur-like smell due to the thiol group.

Comment on solubility

Solubility of 4,5-Dihydro-1H-imidazole-2-thiol

The solubility of 4,5-dihydro-1H-imidazole-2-thiol is an important characteristic that influences its application in various fields of chemistry. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is generally soluble in polar solvents such as water, methanol, and ethanol.
  • Influence of pH: The solubility can vary with changes in pH; being a thiol, the protonation state can significantly affect solubility. For example, in acidic conditions, it may become more soluble.
  • Temperature Effects: Increased temperature usually enhances solubility for many compounds, including 4,5-dihydro-1H-imidazole-2-thiol, as greater kinetic energy allows for better solvation.

It is noteworthy that while it shows good solubility in water due to its polar functionalities, the solubility profile can vary based on the formulation and specific conditions. Thus, it is often advisable to conduct solubility tests under the expected conditions of use.

In summary, 4,5-dihydro-1H-imidazole-2-thiol exhibits favorable solubility in several polar solvents, making it a versatile compound for various applications.

Interesting facts

Interesting Facts about 4,5-Dihydro-1H-Imidazole-2-Thiol

4,5-Dihydro-1H-imidazole-2-thiol, often referred to as a member of the imidazole family, is a fascinating compound that exhibits a variety of intriguing properties and applications. Here are some highlights:

  • Synthetic Versatility: This compound serves as a versatile building block in organic synthesis, paving the way for the formation of more complex molecules. Its structure allows for numerous functional modifications, making it invaluable in chemical research.
  • Biological Relevance: It plays a role in biological systems, particularly in relation to thio-containing compounds. These compounds can participate in various biochemical pathways, contributing to the overall metabolic balance in living organisms.
  • Ligand Properties: The nitrogen atoms in the imidazole ring can coordinate metals, leading to the formation of metal complexes that are essential in catalysis and biological processes such as enzyme function.
  • Antimicrobial Potential: Due to its thiol functionality, this compound exhibits potential antimicrobial properties, which has piqued the interest of researchers looking for new agents in the fight against resistant strains of bacteria.
  • Pharmaceutical Applications: 4,5-Dihydro-1H-imidazole-2-thiol is investigated for its therapeutic potential. Research suggests it could play a role in developing drugs aimed at diseases linked to thiol metabolism.

In summary, the study of 4,5-dihydro-1H-imidazole-2-thiol not only enhances our understanding of imidazole derivatives but also highlights the compound's potential applications in both industrial and medicinal chemistry. As we continue to explore its properties and reactions, the possibilities for innovative uses in science and medicine seem boundless!