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2-(4,5-dihydro-1H-imidazol-2-yl)quinoline

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Identification
Molecular formula
C12H11N3
CAS number
22134-55-2
IUPAC name
2-(4,5-dihydro-1H-imidazol-2-yl)quinoline
State
State

At room temperature, 2-(4,5-dihydro-1H-imidazol-2-yl)quinoline is in a solid state, typically found in a crystalline form.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.15
Boiling point (Celsius)
345.00
Boiling point (Kelvin)
618.15
General information
Molecular weight
197.24g/mol
Molar mass
197.2380g/mol
Density
1.3000g/cm3
Appearence

2-(4,5-dihydro-1H-imidazol-2-yl)quinoline typically appears as a solid compound. Its exact color can vary, but it is often a crystalline solid at room temperature.

Comment on solubility

Solubility of 2-(4,5-dihydro-1H-imidazol-2-yl)quinoline (C12H11N3)

The solubility of 2-(4,5-dihydro-1H-imidazol-2-yl)quinoline is quite intriguing and can be influenced by various factors. Here are some key points regarding its solubility:

  • Polar vs. Nonpolar Solvents: This compound exhibits solubility tendencies that can vary notably between polar and nonpolar solvents. It is often more soluble in nonpolar organic solvents.
  • Hydrogen Bonding: The presence of the imidazole group can facilitate hydrogen bonding with polar solvents, although the overall solubility may still be limited.
  • pH Dependence: Changes in pH can affect the ionization of the nitrogen-containing functional groups in the compound, thereby affecting its solubility.
  • Temperature Factors: In many cases, an increase in temperature can enhance the solubility of organic compounds, including this one, due to increased molecular activity.

In summary, while 2-(4,5-dihydro-1H-imidazol-2-yl)quinoline may have some solubility in polar solvents due to potential hydrogen bonding, its primary solubility features are pronounced in nonpolar environments. As with many organic compounds, understanding the solubility characteristics is crucial for applications in drug formulation and synthesis.

Interesting facts

Interesting Facts about 2-(4,5-dihydro-1H-imidazol-2-yl)quinoline

This intriguing compound, 2-(4,5-dihydro-1H-imidazol-2-yl)quinoline, is a fascinating example of combining two distinct heterocyclic systems: quinoline and imidazole. Both of these moieties are known for their diverse biological activities, lending this compound significant potential in medicinal chemistry.

Biological Relevance

The imidazole ring is notable for its role in numerous biological systems, including:

  • Being a key component of amino acids like histidine.
  • Participating in enzyme catalysis and interactions with metal ions.
  • Exhibiting antibacterial and antifungal properties.

Meanwhile, quinoline derivatives have exhibited:

  • Antimalarial activity.
  • Antitumor properties.
  • Neuroprotective effects.

This combination may result in compounds with unique pharmacological profiles.

Synthetic Considerations

Synthetic pathways to create 2-(4,5-dihydro-1H-imidazol-2-yl)quinoline often involve:

  • Multicomponent reactions, allowing the assembly of complex structures.
  • Functionalization steps to modulate activity and selectivity.

The versatility in synthetic routes highlights the compound's adaptability for further functionalization, crucial for developing targeted therapeutic agents.

Research Potential

As a subject of ongoing research, this compound provides a platform for:

  • Investigating structure-activity relationships (SAR).
  • Exploring its interactions with biological targets, which may lead to novel drug discoveries.

Scholars have noted, *“The unique fusion of quinoline and imidazole opens new avenues in drug design for combating various diseases.”*

In conclusion, 2-(4,5-dihydro-1H-imidazol-2-yl)quinoline stands as an important compound in the field of medicinal chemistry, showcasing the wonderful interplay between different chemical structures and their biological implications.

Synonyms
2-(4,5-dihydro-1H-imidazol-2-yl)quinoline
BU 224
BU-224
BU224
CHEMBL13698
2-(4,5-Dihydroimidaz-2-yl)-Quinoline
NCGC00015130-01
Tocris-0725
Lopac-B-154
Lopac0_000167
SCHEMBL1526637
CHEBI:92967
DTXSID001272339
BDBM50240365
CCG-204262
SDCCGSBI-0050155.P002
NCGC00015130-02
NCGC00015130-03
NCGC00015130-04
NCGC00024750-01
NCGC00024750-02
2-(4,5-Dihydro-1H-imidazol-2-yl)-quinoline
BRD-K55344148-003-01-8
BRD-K55344148-003-02-6
Q27164701