(7-nitroquinolin-8-yl) 4-isopropoxybenzoate
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- Molecular formula
- C19H16N2O5
- CAS Number
- 216302-76-0
- IUPAC Name
- (7-nitro-8-quinolyl) 4-isopropoxybenzoate
- Molecular Weight
- 370.35g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4420g/cm3
- Synonyms
- BRN 1551409
Identification
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.