5-Methyl-1-(2-pyridyl)imidazole-2-thiol

Identification

Molecular formula

C₉H₉N₃S

CAS number

28293-65-8

IUPAC name

5-methyl-1-(2-pyridyl)imidazole-2-thiol

State

The compound is a solid at room temperature. It remains stable under standard conditions and does not readily evaporate or sublimate.

Melting point (Celsius)

153.00

Melting point (Kelvin)

426.15

Boiling point (Celsius)

305.00

Boiling point (Kelvin)

578.15

General information

Molecular weight

177.24g/mol

Molar mass

177.2350g/mol

Density

1.2612g/cm³

Appearence

5-Methyl-1-(2-pyridyl)imidazole-2-thiol appears as a crystalline solid, typically with a yellowish appearance. The compound is known for its distinct and characteristic crystalline form.

Comment on solubility

Solubility of 5-methyl-1-(2-pyridyl)imidazole-2-thiol

5-methyl-1-(2-pyridyl)imidazole-2-thiol, a derivative of imidazole, exhibits intriguing solubility characteristics that are important for its applications in various fields. Here are some key points to consider:

Polar Characteristics: The presence of both a thiol group (-SH) and a pyridine ring contributes to the compound's polarity, which can enhance its solubility in polar solvents.
Solvent Compatibility: It is generally soluble in methanol, ethanol, and warm water, likely due to hydrogen bonding opportunities and the ability to interact favorably with other polar molecules.
Limited Solubility in Non-Polar Solvents: Conversely, solubility in non-polar solvents, such as hexane or benzene, is expected to be low, as the compound favors interactions with polar environments.
Temperature Influence: Raising the temperature may improve solubility; thus, solubility testing under varied conditions is essential for practical applications.

In summary, the solubility of 5-methyl-1-(2-pyridyl)imidazole-2-thiol is influenced by its structural features. Its polar nature allows for significant solubility in polar solvents, making it a versatile compound in various chemical processes.

Interesting facts

Interesting Facts about 5-methyl-1-(2-pyridyl)imidazole-2-thiol

5-methyl-1-(2-pyridyl)imidazole-2-thiol, often referred to simply as a *thiol-containing imidazole compound*, showcases intriguing properties that make it valuable in various fields of research and industry. Here are some notable aspects of this compound:

Biological Relevance: This compound is studied for its potential biological activities, including antioxidant and antimicrobial properties, which can be vital in developing new pharmaceuticals.
Catalytic Applications: 5-methyl-1-(2-pyridyl)imidazole-2-thiol has been recognized for its ability to act as a catalyst in a range of chemical reactions, especially in organic synthesis.
Coordination Chemistry: The compound can form complexes with metal ions, which opens the door to interesting research in the field of coordination chemistry and materials science.
Environmental and Analytical Use: Its unique structure makes it a strong candidate for use in sensors and environmental monitoring systems to detect trace levels of metal ions.

Interestingly, compounds like 5-methyl-1-(2-pyridyl)imidazole-2-thiol play a significant role in the study of transition metals in biological systems, as they often mimic the active sites of various metalloproteins. This connection to biology not only makes such compounds a subject of academic interest but also enhances their applicability in biochemistry and medicine.

As chemistry continuously evolves, compounds like this one remind scientists of the complex intersection of organic chemistry, biochemistry, and real-world applications.