(7-nitro-8-quinolyl) 2,4-dimethoxybenzoate
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- Molecular formula
- C18H14N2O6
- CAS Number
- 402915-85-3
- IUPAC Name
- (7-nitro-8-quinolyl) 2,4-dimethoxybenzoate
- Molecular Weight
- 352.34g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3450g/cm3
- Appearance
- is consistent with many aromatic compounds that have extended conjugated systems.
- Synonyms
- BRN 1553654
Identification
Interesting facts
Interesting Facts about (7-nitro-8-quinolyl) 2,4-dimethoxybenzoate
(7-nitro-8-quinolyl) 2,4-dimethoxybenzoate is a fascinating compound, especially significant in the realm of medicinal chemistry and material science. Here are some intriguing aspects:
- Biomedical Applications: This compound has been researched for its potential pharmacological properties, particularly in the development of drugs targeting various biological pathways. Its structure suggests potential interactions within biological systems, making it a candidate for further study in pharmacokinetics.
- Fluorescent Properties: The quinoline moiety present in the compound endows it with unique photophysical properties. Compounds like this often exhibit fluorescence, making them useful in bioimaging and as fluorescent probes in biological research.
- Structure-Activity Relationship (SAR): The intricate structure of (7-nitro-8-quinolyl) 2,4-dimethoxybenzoate allows for extensive studies into how modifications of its functional groups affect its biological activity. This can lead to the design of more effective derivatives with enhanced potency and selectivity.
- Environmental Implications: As a quinoline derivative, understanding the degradation pathways of this compound in environmental contexts is crucial. Assessing its potential for persistence and bioaccumulation helps chemists mitigate any harmful ecological impacts.
- Historical Significance: Quinoline and its derivatives have a rich history in organic chemistry, being associated with various natural products and synthetic pathways. Investigating compounds like (7-nitro-8-quinolyl) 2,4-dimethoxybenzoate contributes to a broader understanding of chemical synthesis and reactivity.
In summary, the exploration of (7-nitro-8-quinolyl) 2,4-dimethoxybenzoate is not merely academic. As a bridge between theoretical chemistry and practical applications, it holds promise for advancements in both medicinal research and environmental safety, as exemplified by the quote:
"In science, there are no shortcuts to discovery." - A reminder to look deeper into the potential of compounds like this one.