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Benzimidazolium chloride

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Identification
Molecular formula
C11H10ClNO2
CAS number
221503-97-1
IUPAC name
1H-imidazol-3-ium-5-ylmethyl 4-chlorobenzoate;chloride
State
State

At room temperature, the compound exists as a solid.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
258.12g/mol
Molar mass
258.1200g/mol
Density
1.3400g/cm3
Appearence

The compound appears as a white to off-white crystalline powder. It is typically fine-grained and may clump when exposed to moisture.

Comment on solubility

Solubility of 1H-imidazol-3-ium-5-ylmethyl 4-chlorobenzoate;chloride

The compound 1H-imidazol-3-ium-5-ylmethyl 4-chlorobenzoate;chloride displays interesting solubility characteristics:

  • Polarity: Due to the presence of the imidazolium ion and the chloride component, the compound is expected to be polar, which generally enhances solubility in polar solvents.
  • Solvent Compatibility: It is likely soluble in water and other polar solvents like methanol or ethanol, but demonstrate limited solubility in non-polar solvents such as hexane.
  • Temperature Dependency: The solubility may increase with temperature, typical for many ionic compounds, enhancing the dissolution rate in aqueous solutions.
  • Potential for Ion Exchange: The chloride ion may facilitate interactions with various anionic species in solution, potentially leading to complex formation and varying solubility profiles.

In conclusion, the solubility of this compound can vary significantly depending on the solvent environment, temperature, and ionic interactions. Researchers should consider these factors when working with this compound to achieve optimal results in their applications.

Interesting facts

Interesting Facts about 1H-imidazol-3-ium-5-ylmethyl 4-chlorobenzoate;chloride

This intriguing compound falls within the class of imidazolium salts, which are characterized by their unique ring structure and fascinating properties. Here are some interesting tidbits that highlight its significance in chemistry:

  • Functional Versatility: Imidazolium salts are often utilized as ionic liquids and serve as versatile reagents in organic synthesis. Their tunable nature makes them suitable for various applications, including catalysis and electrochemistry.
  • Biological Relevance: This compound and its derivatives are of interest in the field of medicinal chemistry. Certain imidazolium compounds have shown anti-cancer, antibacterial, and antifungal activities, making them valuable for pharmaceutical research.
  • Solubility in Water: The presence of the imidazolium cation contributes to **increased solubility** in polar solvents, which is beneficial for many applications in biochemical reactions.
  • Electrochemical Properties: The stability and conductivity of imidazolium salts make them attractive for use in energy storage devices, such as batteries and supercapacitors. Their ionic nature allows for efficient charge transfer.
  • Contribution to Green Chemistry: As a part of the growing field of green chemistry, imidazolium salts contribute to the development of more sustainable chemical processes, reducing the environmental impact of chemical manufacturing.

In summary, 1H-imidazol-3-ium-5-ylmethyl 4-chlorobenzoate;chloride exemplifies the fascinating intersection of structure and function in modern chemistry. Its numerous applications span from synthetic chemistry to potential therapeutic uses, underscoring the importance of researching and understanding such compounds.

Synonyms
BENZOIC ACID, p-CHLORO-, IMIDAZOL-4-YLMETHYL ESTER, MONOHYDROCHLORIDE
18429-75-9
p-Chlorobenzoic acid imidazol-4-ylmethyl ester hydrochloride
Imidazole-4-methanol, p-chlorobenzoate (ester), hydrochloride