2,2,3,3-tetrafluoropropyl 3-(aziridin-1-yl)propanoate
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- Molecular formula
- C9H12F4NO2
- CAS Number
- Not Available
- IUPAC Name
- 2,2,3,3-tetrafluoropropyl 3-(aziridin-1-yl)propanoate
- Molecular Weight
- 267.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2240g/cm3
- Synonyms
- 1-AZIRIDINEPROPIONIC ACID, 2, 2, 3, 3-TETRAFLUOROPROPYL ESTER
Identification
Interesting facts
Interesting Facts about 2,2,3,3-Tetrafluoropropyl 3-(aziridin-1-yl)propanoate
2,2,3,3-Tetrafluoropropyl 3-(aziridin-1-yl)propanoate is a fascinating compound that exemplifies the intricate intersection of organic chemistry and medicinal applications. Here are some intriguing aspects of this compound:
- Fluorinated Properties: The presence of four fluorine atoms in this compound enhances its chemical stability and lipophilicity, which can significantly influence its interaction with biological systems.
- Aziridine Ring: The aziridine moiety is a three-membered cyclic amine that plays a crucial role in medicinal chemistry. Its unique structure can facilitate ring-opening reactions, making it a versatile building block in drug synthesis.
- Potential Applications: This compound could be explored for use in developing novel pharmaceutical agents. Its unique functional groups may contribute to specific interactions with biological targets, aiding in drug design.
- Research Interest: Compounds like this one are often the subject of research due to their potential as anti-cancer agents, where the aziridine component may be particularly effective.
- Environmental Considerations: The incorporation of fluorinated compounds is both beneficial for enhancing performance in some applications and raises concerns regarding environmental impact and biodegradability. Understanding these aspects is crucial for future studies.
As scientists continue to explore the realms of chemistry, compounds such as 2,2,3,3-tetrafluoropropyl 3-(aziridin-1-yl)propanoate challenge our understanding of structure-activity relationships and inspire innovative approaches to drug development.