(7-nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate
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- Molecular formula
- C19H13N3O6
- CAS Number
- 123456-78-9
- IUPAC Name
- (7-nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate
- Molecular Weight
- 370.34g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4000g/cm3
Identification
Interesting facts
Interesting Facts about (7-Nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate
(7-Nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate is a fascinating compound that plays an important role in various fields of research and application. Here are some key points that highlight its significance:
- Structural Complexity: This compound features a complex structure that includes a nitro-substituted quinoline moiety fused with a phenyl group. The interplay of various functional groups contributes to its unique chemical properties.
- Biological Activity: Research has indicated that compounds similar to (7-nitro-8-quinolyl) derivatives can exhibit significant biological activities, including antibacterial and antitumor properties. This makes it a valuable candidate for pharmaceutical development.
- Potential Applications: The compound may find applications in the fields of organic synthesis and medicinal chemistry. Its structural features can be exploited to design new drugs and explore novel therapeutic pathways.
- Fluorescence Properties: Many quinoline derivatives, including this compound, are known for their interesting fluorescence properties. These characteristics make them suitable for use as fluorescent probes in biological and chemical sensing applications.
- Research Significance: The study of such compounds not only enhances our understanding of organic chemistry but also paves the way for the discovery of new methodologies in synthesizing complex molecules.
In summary, (7-nitro-8-quinolyl) 2-methyl-3-(2-nitrophenyl)prop-2-enoate is more than just a chemical compound; it is a bridge to understanding complex interactions within biological systems and offers potential for innovative applications in science and medicine.