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1,3-bis(1-methylquinolin-1-ium-6-yl)urea

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Identification
Molecular formula
C21H20N4O
CAS number
215868-57-0
IUPAC name
1,3-bis(1-methylquinolin-1-ium-6-yl)urea
State
State

The compound is typically found in a solid state at room temperature. It is a high melting-point substance, indicating strong intermolecular forces, likely due to π-π interactions between the aromatic moieties and hydrogen bonding potential within the urea functional group.

Melting point (Celsius)
275.00
Melting point (Kelvin)
548.00
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.00
General information
Molecular weight
338.39g/mol
Molar mass
338.3870g/mol
Density
1.3140g/cm3
Appearence

This compound typically appears as a crystalline powder. The color of the compound can vary depending on its purity, ranging from almost white to off-white. It may also exhibit a slight shimmer or gloss under certain lighting conditions due to its crystalline nature. Being a complex organic compound, it is not generally encountered in everyday environments but rather in specialized research or applications.

Comment on solubility

Solubility of 1,3-bis(1-methylquinolin-1-ium-6-yl)urea

The solubility of 1,3-bis(1-methylquinolin-1-ium-6-yl)urea can be a fascinating topic due to the influence of its unique structure. This compound, characterized by its dual quinolin-1-ium cations, plays a significant role in determining its solubility in various solvents.

Typically, solubility is influenced by a number of factors:

  • Polarity: Compounds with polar functional groups tend to dissolve better in polar solvents (like water), while non-polar groups favor non-polar solvents (like hexane).
  • Hydrogen Bonding: The presence of urea groups can facilitate hydrogen bonding, enhancing solubility in polar solvents.
  • Ionization: The ionizable nature of the quinolin-1-ium moiety may lead to increased solubility in aqueous solutions due to the formation of charged species.

For 1,3-bis(1-methylquinolin-1-ium-6-yl)urea:

  • It is likely to have enhanced solubility in polar organic solvents.
  • Its solubility in water may be moderate, depending on the pH and ionic strength of the solution due to the quaternary ammonium ions.
  • Increasing temperature may also affect solubility, as seen in many organic compounds.

In summary, the solubility of 1,3-bis(1-methylquinolin-1-ium-6-yl)urea is a complex interplay of structural characteristics and environmental conditions. Understanding these factors can help in predicting its behavior in various chemical and biological contexts.

Interesting facts

Exploring 1,3-bis(1-methylquinolin-1-ium-6-yl)urea

1,3-bis(1-methylquinolin-1-ium-6-yl)urea is a fascinating compound with notable applications in various fields, particularly in the realm of medicinal chemistry and materials science.

Key Features and Applications:

  • Quinoline Framework: This compound features a quinoline structure, which is well-known for its role in the synthesis of biologically active compounds.
  • Anti-cancer Activity: Research indicates that derivatives of quinoline exhibit promising anti-cancer properties, making this compound a subject of interest for drug development.
  • Fluorescent Properties: The incorporation of quinoline moieties leads to significant fluorescence, which can be utilized in imaging techniques and sensor applications.
  • Potential as a Biochemical Probe: The unique structural characteristics of this compound may allow it to function as a probe for studying biological systems.

Notably, the presence of the urea group enhances the compound's ability to engage in hydrogen bonding, potentially influencing its solubility and reactivity in biological environments. As a scientist or chemistry student delving into this compound, one could explore:

  1. The mechanism of action behind its biological activity.
  2. The synthetic pathways for producing this compound and its derivatives.
  3. The therapeutic potential of quinoline-based compounds.

In conclusion, 1,3-bis(1-methylquinolin-1-ium-6-yl)urea exemplifies the intersection of organic chemistry and pharmacology. Its diverse applications underlie the importance of exploring complex chemical structures in advancing medical science. As the quote goes, “Chemistry is the soul of medicine,” highlighting the significance of compounds like this in improving human health.

Synonyms
Quinuronium
14910-31-7
Quinolinium, 6,6'-(carbonyldiimino)bis(1-methyl-
Quinolinium, 6,6'-ureylenebis(1-methyl-
1,3-bis(1-methylquinolin-1-ium-6-yl)urea
324LL33THV
6,6/'-(Carbonylbisimino)bis(1-methylquinolinium)
BRN 3710776
UNII-324LL33THV
6,6'-(Carbonyldiimino)bis(1-methylquinolinium)
QUINURONIUM ION
QUINURONIUM CATION
DTXSID00164176
N,N'-DIMETHYL-1,3-DI-6-QUINOLYLUREA
Q27256137