Skip to main content

Chloro(3-(2,5-dioxoimidazolidin-1-yl)-2-methoxypropyl)mercury

ADVERTISEMENT
Identification
Molecular formula
C8H11ClHgNO4
CAS number
1182-70-5
IUPAC name
chloro-[3-(2,5-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury
State
State

At room temperature, chloro(3-(2,5-dioxoimidazolidin-1-yl)-2-methoxypropyl)mercury is a solid. Due to its relatively high density, it is notable for a heavier, more compact physicality typical of mercury-containing compounds.

Melting point (Celsius)
122.00
Melting point (Kelvin)
395.15
Boiling point (Celsius)
256.00
Boiling point (Kelvin)
529.15
General information
Molecular weight
440.30g/mol
Molar mass
440.3030g/mol
Density
3.7100g/cm3
Appearence

Chloro(3-(2,5-dioxoimidazolidin-1-yl)-2-methoxypropyl)mercury typically appears as a crystalline solid, showcasing a white to light yellow coloration. Its crystalline structure can vary slightly depending on the specific conditions of its synthesis and storage.

Comment on solubility

Solubility of Chloro-[3-(2,5-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury

The solubility of chloro-[3-(2,5-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury can be intriguing, primarily because of the complexities introduced by the mercury component. When considering solubility, it is essential to take into account the following factors:

  • Polarity: The presence of both chloro and methoxy functional groups suggests varying polarity, affecting how this compound interacts with solvents.
  • Complexation: Mercury tends to form complexes with different ligands, which can either enhance or inhibit solubility in various solvents.
  • Solvent Effects: Solubility may vary greatly depending on whether the medium is polar (like water) or non-polar (like organic solvents).
  • Temperature: Increasing temperature often increases solubility for many compounds, yet specific interactions in this compound may deviate from the norm.

In general, mercury compounds have a notorious reputation for poor solubility in aqueous solutions, mainly due to their heavy metal character. Furthermore, chloro- and methoxy-substituents might add a nuanced layer that potentially alters solubility dynamics. As a result, it's imperative to conduct empirical testing to determine the precise solubility profile of this unique compound.

Ultimately, understanding the solubility of chloro-[3-(2,5-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury requires careful analysis and consideration of its chemical interactions in various environments.

Interesting facts

Interesting Facts about Chloro-[3-(2,5-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury

Chloro-[3-(2,5-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury is an intriguing organomercury compound that presents a unique blend of properties and potential applications. Below are some fascinating aspects of this compound:

  • Organomercury Chemistry: This compound belongs to the family of organomercury compounds, which are organic molecules that contain mercury. These compounds are known for their diverse reactivity and applications in various fields, including medicinal chemistry and biochemistry.
  • Biological Activity: Organomercury compounds often exhibit interesting biological activity. Chloro-[3-(2,5-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury has garnered attention for its potential roles in biological systems, especially in the context of antimicrobial and antiviral properties.
  • Ligand Binding: The imidazolidinone moiety present in the molecule can interact with various biological macromolecules, including proteins and nucleic acids. This interaction can lead to significant changes in cellular function, making the study of such compounds important in drug design.
  • Environmental Considerations: Mercury is a well-known pollutant with serious environmental and health impacts. Understanding the behavior of compounds like this one is essential for assessing their safety and risks associated with mercury exposure.
  • Research Interest: There is ongoing research to explore the reactivity, stability, and biological effects of this compound and similar organomercury derivatives. Insights gained from such studies may lead to new therapeutic agents or better understanding of their toxicity.
  • Quote from a Renowned Chemist: “The elegance of organomercury compounds lies in their ability to bridge organic chemistry with biological systems, presenting both opportunities and challenges.”

In summary, chloro-[3-(2,5-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury is more than just a chemical compound; it represents a fascinating intersection of chemistry, biology, and environmental science. Researching such compounds is crucial not only for the advancement of scientific knowledge but also for ensuring public safety.

Synonyms
3-(3-Chloromercuri-2-methoxy-1-propyl)hydantoin
3367-29-1
BRN 0650751
MERCURY, CHLORO((3-(2,4-DIOXO-3-IMIDAZOLIDINYL)-2-METHOXY)PROPYL)-