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Mepacrine Dihydrochloride

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Identification
Molecular formula
C23H30Cl3N3O
CAS number
130-26-7
IUPAC name
(4-chlorophenyl)-[1-(2-morpholin-4-ium-4-ylethyl)pyrrol-2-yl]methanone;chloride
State
State

This compound is typically found in a solid state at room temperature. It is highly hygroscopic and can absorb moisture from the surroundings.

Melting point (Celsius)
117.00
Melting point (Kelvin)
390.00
Boiling point (Celsius)
246.00
Boiling point (Kelvin)
519.00
General information
Molecular weight
496.94g/mol
Molar mass
496.9360g/mol
Density
1.3200g/cm3
Appearence

This compound appears as a crystalline solid with a light yellow or slightly brownish color. It is usually odorless and is very hygroscopic.

Comment on solubility

Solubility of (4-chlorophenyl)-[1-(2-morpholin-4-ium-4-ylethyl)pyrrol-2-yl]methanone;chloride

The solubility of the compound (4-chlorophenyl)-[1-(2-morpholin-4-ium-4-ylethyl)pyrrol-2-yl]methanone;chloride is influenced by its complex structure and the presence of charged functional groups. In general, the solubility of a compound can be understood by considering a few key factors:

  • Polarity: The presence of the morpholine and chloride ions significantly enhances the polarity of the compound, making it more soluble in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules increases solubility, especially with the amino moiety present in the morpholine.
  • Chain Length: The ethyl chain can provide some hydrophobic character, which may affect solubility in non-polar solvents.
  • Salt Formation: As a chloride salt, it may display better solubility profiles compared to its neutral form, often showing increased solubility in aqueous environments.

In conclusion, while the exact solubility value can vary depending on the specific conditions, one can generally expect this compound to be highly soluble in polar solvents due to its ionic nature and ability to engage in hydrogen bonding.

Interesting facts

Interesting Facts about (4-chlorophenyl)-[1-(2-morpholin-4-ium-4-ylethyl)pyrrol-2-yl]methanone;chloride

This intriguing compound exhibits a remarkable blend of pharmaceutical and chemical properties that make it a topic of interest in the scientific community. Here are some fascinating insights:

  • Pharmaceutical Applications: The presence of the morpholine group in its structure hints at potential applications in medicinal chemistry, particularly in drug design and development. Such compounds are often investigated for their biological activities.
  • Mechanism of Action: Compounds with similar structures may interact with specific receptors in the body. Understanding how this compound functions at the molecular level can unveil new therapeutic targets.
  • Chlorine Atom Significance: The 4-chloro substitution is not just a structural feature; it can significantly influence the compound’s electronegativity and reactivity. This makes it a useful building block in synthesis.
  • Chemistry of Pyrrole: Pyrrole rings are known for their role in various natural products and bioactive compounds. The functionality of this compound opens doors for research into new synthetic pathways.
  • Multi-Functional Traits: Due to its complex structure, researchers are exploring this compound for multiple functionalities, from insecticidal properties to as potential agents in cancer treatment.

In the words of a leading chemist, "The pursuit of understanding compounds like (4-chlorophenyl)-[1-(2-morpholin-4-ium-4-ylethyl)pyrrol-2-yl]methanone is not just about knowing their structure; it’s about unlocking the potential they hold for future applications."

Overall, compounds like this one represent a convergence of chemistry and biology, illustrating how intricate molecular designs can lead to significant advancements in science.

Synonyms
2-(p-Chlorobenzoyl)-1-(2-morpholinoethyl)pyrrole monohydrochloride
14415-66-8
KETONE, p-CHLOROPHENYL 1-(2-MORPHOLINOETHYL)PYRROL-2-YL, HYDROCHLORIDE