2-Fluoroethyl 2-aminoacetate
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- Molecular formula
- C4H8FNO2
- CAS Number
- 459-40-3
- IUPAC Name
- 2-fluoroethyl 2-aminoacetate
- Molecular Weight
- 135.12g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1960g/cm3
- Synonyms
- 2-fluoroethyl glycinate
Identification
Interesting facts
Interesting Facts About 2-Fluoroethyl 2-Aminoacetate
2-Fluoroethyl 2-aminoacetate, a fascinating compound, plays a vital role in the field of medicinal chemistry and synthetic organic chemistry. Here are some intriguing aspects of this compound:
- Functional Versatility: The presence of both fluoro and amino groups in the structure allows 2-fluoroethyl 2-aminoacetate to serve as an important building block in the synthesis of more complex molecules and pharmaceuticals.
- Biological Significance: The fluorine atom in the compound often enhances biological activity and metabolic stability, making it an attractive candidate for drug discovery.
- Research Applications: This compound may be utilized in studying enzyme activities, receptor interactions, and other biological processes due to its specific functional groups, making it a valuable tool in biochemical research.
- Synthesis Pathways: Chemists have developed various synthesis pathways for 2-fluoroethyl 2-aminoacetate, showcasing its accessibility for laboratory procedures and industrial applications.
- Influence on Properties: The introduction of fluorine can dramatically alter the physicochemical properties of the compound, including its lipophilicity and binding affinity, which can be crucial for designing effective therapeutics.
As one delves deeper into its potential applications and significance, it's clear that 2-fluoroethyl 2-aminoacetate provides a fascinating intersection of fundamental chemistry and practical application, contributing to advancements in both academic and industrial settings.