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1-Methylimidazole-2-thiol

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Identification
Molecular formula
C4H6N2S
CAS number
870-39-7
IUPAC name
1-methylimidazole-2-thiol
State
State

At room temperature, 1-Methylimidazole-2-thiol is in a solid state, forming yellow crystals. It is generally stable and manifests as a powdery substance.

Melting point (Celsius)
26.00
Melting point (Kelvin)
299.10
Boiling point (Celsius)
268.50
Boiling point (Kelvin)
541.60
General information
Molecular weight
114.17g/mol
Molar mass
114.1670g/mol
Density
1.2500g/cm3
Appearence

1-Methylimidazole-2-thiol presents as a yellow crystalline solid. It has a distinctive odor, commonly associated with compounds containing sulfur.

Comment on solubility

Solubility of 1-methylimidazole-2-thiol

1-methylimidazole-2-thiol (C4H6N2S) exhibits notable solubility characteristics that can be understood through several key factors:

  • Polar Nature: The presence of both nitrogen and sulfur in the molecular structure contributes to a polar character, which generally enhances solubility in polar solvents.
  • Water Solubility: 1-methylimidazole-2-thiol is likely soluble in water due to its ability to form hydrogen bonds, making it a suitable candidate for various aqueous applications.
  • Organic Solubility: It tends to be soluble in common organic solvents such as ethanol and methanol, demonstrating versatility in solubility.

In summary, the solubility of 1-methylimidazole-2-thiol is influenced by its polar attributes and structural functionalities, promoting compatibility with both polar and non-polar solvent systems. Understanding these solubility traits is essential for applications in scientific research and industrial processes, providing a baseline for predicting behavior in different environments.

Interesting facts

Interesting Facts about 1-Methylimidazole-2-thiol

1-Methylimidazole-2-thiol is a fascinating compound with a variety of applications in both industry and research. Here are some intriguing aspects of this compound:

  • Chemical Structure: This compound contains a five-membered ring structure characteristic of imidazoles, which contributes to its unique chemical properties and reactivity.
  • Thiol Group: The presence of the thiol (-SH) group gives this compound distinctive behaviors, making it a versatile agent in nucleophilic substitution reactions and as a reducing agent.
  • Biological Activity: 1-Methylimidazole-2-thiol has been studied for its potential roles in biological systems, including metabolic processes. Its derivatives can be significant in pharmaceuticals.
  • Industrial Use: This compound finds applications in the synthesis of various materials, including polymers and catalysts, showcasing its importance in chemical manufacturing.
  • Research Interest: Given its unique properties, 1-Methylimidazole-2-thiol is actively researched within the field of organic chemistry and medicinal chemistry, often being a part of studies related to new compound formation.

It is often said that "unique structures lead to unique properties," and this notion holds true for 1-Methylimidazole-2-thiol, making it a compound worth exploring for scientists and students alike!