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(7-nitroquinolin-8-yl) 4-isopropoxybenzoate

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Identification
Molecular formula
C19H16N2O5
CAS number
216302-76-0
IUPAC name
(7-nitro-8-quinolyl) 4-isopropoxybenzoate
State
State

At room temperature, this compound is a solid. It is typically stable under normal conditions and is used in laboratories for organic synthesis and as a reagent.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
470.00
Boiling point (Kelvin)
743.15
General information
Molecular weight
370.35g/mol
Molar mass
370.3560g/mol
Density
1.4420g/cm3
Appearence

The compound typically appears as a crystalline solid or powder with a slight yellowish tinge due to the presence of the nitro group. It is often used in chemical synthesis and research applications.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 4-isopropoxybenzoate

The solubility of (7-nitro-8-quinolyl) 4-isopropoxybenzoate can be influenced by various factors, including its molecular structure and the nature of the surrounding solvent. In general, this compound exhibits a degree of solubility in organic solvents due to the presence of the isopropoxy group, which can enhance solvating interactions.

Here are some key points regarding its solubility:

  • Polar solvents: The compound may have limited solubility in polar solvents like water, given the hydrophobic characteristics of the quinoline moiety.
  • Non-polar solvents: Conversely, it is more likely to dissolve in non-polar organic solvents such as dichloromethane or ether.
  • Temperature dependence: The solubility may increase with temperature, a characteristic common to many organic compounds. As temperature rises, molecular motion enhances solute-solvent interactions.

Understanding the solubility of (7-nitro-8-quinolyl) 4-isopropoxybenzoate is crucial for its application in various chemical processes. As with many compounds, it is often stated that “like dissolves like,” which emphasizes the importance of matching polarity between solute and solvent for optimal solubility.

In summary, pay careful attention to the choice of solvent when working with this compound, as it plays a critical role in achieving desired solubility outcomes.

Interesting facts

Interesting Facts about (7-nitro-8-quinolyl) 4-isopropoxybenzoate

(7-nitro-8-quinolyl) 4-isopropoxybenzoate is a fascinating compound with several noteworthy attributes. Here are some key points that illustrate its significance in the field of chemistry:

  • Versatile Applications: This compound is primarily utilized in the field of medicinal chemistry, particularly for its potential as an antibacterial agent. Its unique structure allows for investigations into new drug design.
  • Quinoline Derivative: Being a quinoline derivative, it shares many of the properties associated with this class of compounds, including its potential biological activity. Quinoline derivatives are known for their roles in various pharmaceutical applications.
  • Research Interest: The presence of a nitro group in its structure may enhance its interaction with biological systems. Researchers often focus on nitro compounds due to their wide-ranging effects and applications in synthetic and medicinal chemistry.
  • Structure-Activity Relationship (SAR): The investigation of (7-nitro-8-quinolyl) 4-isopropoxybenzoate allows scientists to explore the relationship between its structural features and biological activity. This is crucial for understanding how modifications to its structure can affect its performance as a drug.
  • Environmental Impact: Like many synthetic compounds, understanding the environmental degradation and toxicity of (7-nitro-8-quinolyl) 4-isopropoxybenzoate is essential. Ongoing studies into its biocompatibility and ecological effects contribute to safer chemical practices.

The exploration of this compound opens up numerous avenues for research and development, making it a notable subject in advanced organic and medicinal chemistry studies. Overall, (7-nitro-8-quinolyl) 4-isopropoxybenzoate stands as an example of how intricate chemical structures can lead to significant biological and industrial advancements.

Synonyms
BRN 1551409
BENZOIC ACID, p-ISOPROPOXY-, 7-NITRO-8-QUINOLYL ESTER
8-Quinolinol, 7-nitro-, p-isopropoxybenzoate
29002-44-6
p-Isopropoxybenzoic acid 7-nitro-8-quinolyl ester
DTXSID60183207
RefChem:327949
DTXCID30105698
SCHEMBL4458673