5-Methyl-5-phenyl-1,4-dihydroimidazole-2-thiol

Identification

Molecular formula

C₁₀H₁₂N₂S

CAS number

2346-24-9

IUPAC name

5-methyl-5-phenyl-1,4-dihydroimidazole-2-thiol

State

This compound is in a solid state at room temperature. The solid is stable under normal temperatures and pressures.

Melting point (Celsius)

128.00

Melting point (Kelvin)

401.15

Boiling point (Celsius)

545.60

Boiling point (Kelvin)

818.80

General information

Molecular weight

204.29g/mol

Molar mass

204.2920g/mol

Density

1.2260g/cm³

Appearence

5-Methyl-5-phenyl-1,4-dihydroimidazole-2-thiol is typically a crystalline solid with a pale yellow color. It may have a slight sulfurous odor due to the thiol group.

Comment on solubility

Solubility of 5-methyl-5-phenyl-1,4-dihydroimidazole-2-thiol

The solubility of 5-methyl-5-phenyl-1,4-dihydroimidazole-2-thiol (C₁₀H₁₂N₂S) can be influenced by various factors. Understanding its solubility behavior is crucial for applications in pharmaceuticals and chemical syntheses.

Key Factors Affecting Solubility:

Polarity: The presence of the thiol (-SH) group increases the polarity of the molecule, which can enhance solubility in polar solvents.
Hydrophobic Characteristics: The phenyl and methyl groups contribute to hydrophobic interactions, which can lead to lower solubility in water.
Temperature: Typically, increasing temperature can elevate solubility for many compounds; however, this may vary based on the specific properties of the thiol compound.

In practical terms, this compound is expected to have moderate solubility in organic solvents such as ethanol and acetone, while its solubility in water may be considerably less due to its hydrophobic regions.

In conclusion, understanding the solubility of 5-methyl-5-phenyl-1,4-dihydroimidazole-2-thiol is essential for optimizing its use in various chemical environments and formulations.

Interesting facts

Interesting Facts about 5-methyl-5-phenyl-1,4-dihydroimidazole-2-thiol

5-methyl-5-phenyl-1,4-dihydroimidazole-2-thiol is a fascinating compound that falls into the category of imidazole derivatives, which are notable for their diverse applications in various scientific fields. Here are some captivating aspects:

Biological Applications: This compound is of interest in pharmacology due to its potential as a drug candidate. Its structure allows for interactions with biological systems that could lead to developments in medicinal chemistry.
Thiols in Chemistry: The presence of a thiol group (–SH) makes this compound particularly important. Thiols are often involved in biochemical reactions and can act as reducing agents, making them pivotal in enzyme function and metabolic processes.
Synthetic Pathways: The synthesis of 5-methyl-5-phenyl-1,4-dihydroimidazole-2-thiol utilizes creative reaction mechanisms, offering opportunities for chemists to explore novel methodologies. This encourages the development of new synthetic strategies in imidazole chemistry.
Versatile Framework: Its unique structure enables modifications that facilitate the study of structure-activity relationships, making it a valuable compound for research in drug design and development.
Potential in Material Science: Beyond biomedicine, compounds like 5-methyl-5-phenyl-1,4-dihydroimidazole-2-thiol are being explored for their prospects in materials science. The thiol functionality can lead to applications in polymerization processes and coordination with metal ions.

Overall, 5-methyl-5-phenyl-1,4-dihydroimidazole-2-thiol is a prime example of how a complex organic compound can hold significant implications in various fields, fostering innovation and multidisciplinary research.