Interesting facts
Interesting Facts about N-[3-(dimethylamino)propyl]-2-(4-oxo-2-phenyl-chromen-7-yl)oxy-acetamide
N-[3-(dimethylamino)propyl]-2-(4-oxo-2-phenyl-chromen-7-yl)oxy-acetamide, often abbreviated in research contexts, is a fascinating compound with numerous applications in the field of medicinal chemistry. Here are some notable aspects:
- Structure and Functionality: The compound features a unique combination of a chromen-7-yl moiety and an acetamide functional group. This structural diversity contributes to its potential biological activities.
- Biological Significance: Compounds that contain both chromene and amine derivatives are often explored for their pharmacological properties. This particular compound may exhibit interesting effects on various biological systems, including anti-inflammatory and anticancer activities.
- Synthetic Pathways: The synthesis of such complex compounds typically involves intricate organic reactions. Chemists have creatively utilized various methods such as quaternization and amide bond formation to produce this compound, showcasing the versatility of organic synthesis techniques.
- Research Potential: Ongoing studies of N-[3-(dimethylamino)propyl]-2-(4-oxo-2-phenyl-chromen-7-yl)oxy-acetamide are likely to uncover even more about its properties, enhancing our understanding of how structural modifications can lead to variations in biological activity.
- Interdisciplinary Implications: The compound serves as a bridge between organic chemistry and pharmacology, making it a relevant subject in discussions surrounding drug design and discovery.
As a compound of interest, N-[3-(dimethylamino)propyl]-2-(4-oxo-2-phenyl-chromen-7-yl)oxy-acetamide is poised to contribute to our understanding of complex chemical interactions in biological systems. Its study could unveil new therapeutic agents that leverage the therapeutic potential embedded in its molecular structure.
Synonyms
FLA 22
BRN 1298536
607-75-0
(gamma-Dimethylaminopropyl)-amid der flavon-7-oxyessigsaeure [German]
N-(3-(Dimethylamino)propyl)-2-((4-oxo-2-phenyl-4H-1-benzopyran-7-yl)oxy)acetamide
DTXSID20209518
Flavon-7-oxyessigsaeure-(gamma-dimethylaminopropyl)amid [German]
Acetamide, N-(3-(dimethylamino)propyl)-2-((4-oxo-2-phenyl-4H-1-benzopyran-7-yl)oxy)-
Flavon-7-oxyessigsaeure-(gamma-dimethylaminopropyl)amid
(gamma-Dimethylaminopropyl)-amid der flavon-7-oxyessigsaeure
DTXCID70132009
5-18-02-00264 (beilstein handbook reference)
Solubility of N-[3-(dimethylamino)propyl]-2-(4-oxo-2-phenyl-chromen-7-yl)oxy-acetamide
The solubility of N-[3-(dimethylamino)propyl]-2-(4-oxo-2-phenyl-chromen-7-yl)oxy-acetamide can be influenced by several factors, notably its chemical structure and functional groups. This compound contains both hydrophilic (water-attracting) and hydrophobic (water-repelling) characteristics, which can lead to varying solubility in different solvents.
Generally, an increase in temperature can enhance the solubility of solid compounds in solvents, allowing for better dissolution of N-[3-(dimethylamino)propyl]-2-(4-oxo-2-phenyl-chromen-7-yl)oxy-acetamide in certain conditions.
As concentration increases, the solubility can also be affected. This compounds interactions may lead to saturation at certain levels, leading to potential precipitation if the solution exceeds its solubility limit.
In summary, the solubility of N-[3-(dimethylamino)propyl]-2-(4-oxo-2-phenyl-chromen-7-yl)oxy-acetamide strikes a balance between its hydrophilic and hydrophobic features, making it an intriguing compound in terms of solubility behavior in various solvents.