Interesting facts
Interesting Facts about Ethyl 8-Fluoro-3-oxo-octanoate
Ethyl 8-fluoro-3-oxo-octanoate is a fascinating compound in the realm of organic chemistry, particularly recognized for its diverse applications and unique properties. Here are some compelling facts:
- Fluorine Influence: The presence of the F atom significantly enhances the chemical and biological characteristics of this compound. Fluorine can affect the compound's reactivity and stability, making it of interest in pharmaceuticals.
- Versatile Synthesis: Ethyl 8-fluoro-3-oxo-octanoate can be synthesized through various methods, often involving the acylation of ethyl octanoate. This versatility allows chemists to explore different pathways and optimize yield.
- Biological Applications: The structural framework of this compound suggests potential applications in drug development. Compounds similar to ethyl 8-fluoro-3-oxo-octanoate are studied for their biological activity, including anti-inflammatory and antimicrobial effects.
- Incorporation in Research: Scientists are investigating this compound and its derivatives for their role in various chemical reactions, particularly as intermediates in the synthesis of more complex molecules.
- Contribution to Flavor Chemistry: Compounds containing ester groups are often evaluated within the realm of flavor chemistry, contributing to the sensory profiles of various products. The unique attributes of ethyl 8-fluoro-3-oxo-octanoate might offer intriguing flavor characteristics.
As a compound that beautifully bridges different aspects of organic chemistry and applied sciences, ethyl 8-fluoro-3-oxo-octanoate exemplifies how subtle changes in molecular structure can lead to profound implications in both research and industrial applications. It opens the door to exciting developments in chemical synthesis and pharmaceutical research.
Synonyms
Ethyl 8-fluoro-3-oxooctanoate
333-56-2
BRN 1775525
Ethyl omega-fluoro-3-oxooctanoate
8-Fluoro-3-oxo-octanoic acid ethyl ester
OCTANOIC ACID, 8-FLUORO-3-OXO-, ETHYL ESTER
DTXSID30186922
4-03-00-01611 (Beilstein Handbook Reference)
8-Fluoro-3-oxooctanoic acid ethyl ester
SCHEMBL3104038
DTXCID70109413
Solubility of Ethyl 8-Fluoro-3-Oxo-Octanoate
Ethyl 8-fluoro-3-oxo-octanoate, with the chemical formula C13H21F1O3, exhibits interesting solubility characteristics influenced by both its functional groups and overall structure.
In Water
This compound is generally considered to have low solubility in water due to:
As a result, it might be classified as a poorly soluble compound in aqueous environments.
In Organic Solvents
However, ethyl 8-fluoro-3-oxo-octanoate displays greater solubility in many organic solvents, specifically:
This increased solubility can be attributed to the molecule's ability to engage in Van der Waals interactions and dipole-dipole interactions with organic solvent molecules.
Conclusion
In summary, while ethyl 8-fluoro-3-oxo-octanoate is less soluble in water, it finds considerable solubility in organic solvents, making it suitable for various applications in organic chemistry and synthesis.