2-(2-Nitrophenyl)-3-phenylpropenoic acid
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- Molecular formula
- C15H11NO4
- CAS Number
- 54849-56-2
- IUPAC Name
- 3-(2-nitrophenyl)-2-phenyl-prop-2-enoic acid
- Molecular Weight
- 255.25g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3880g/cm3
- Synonyms
- 3-(o-Nitrophenyl)-2-phenylpropenoic acid
Identification
Interesting facts
Interesting Facts about 3-(2-nitrophenyl)-2-phenyl-prop-2-enoic acid
3-(2-nitrophenyl)-2-phenyl-prop-2-enoic acid, commonly referred to in research contexts as a derivative of cinnamic acid, showcases intriguing properties and applications:
- Application in Organic Synthesis: This compound acts as a significant intermediate in various chemical syntheses. It can be utilized in the preparation of more complex molecules, particularly in pharmaceuticals.
- Biological Activity: Some studies suggest potential biological activities, including anti-inflammatory and anti-cancer properties, making it a subject of interest in medicinal chemistry.
- Electronic Properties: Its structure contains both electron-withdrawing (the nitro group) and electron-donating (the phenyl group) elements, which can influence its reactivity and interaction with different chemical environments.
- Research Importance: Due to its unique structural features, it serves as a pivotal model in the study of structure-activity relationships (SAR) in various compounds.
- Synthesis Techniques: The synthesis often involves modern organic synthesis techniques, highlighting the relevance of methodologies like Suzuki coupling and other cross-coupling reactions.
In the words of a researcher, “Understanding this compound not only enhances our grasp of organic chemistry but also opens doors to potential applications in drug development.”
It exemplifies the interconnectedness of organic compounds and their significant roles in advancing scientific knowledge and technological innovations.