Phenethylcarbamate
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- Molecular formula
- C11H15NO2
- CAS Number
- 1421-86-5
- IUPAC Name
- ethyl N-(1-phenylethylamino)carbamate
- Molecular Weight
- 206.26g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1550g/cm3
- Synonyms
- Carbenzide
Identification
Interesting facts
Interesting Facts about Ethyl N-(1-phenylethylamino)carbamate
Ethyl N-(1-phenylethylamino)carbamate is a fascinating compound that has gained attention within various fields of chemistry and pharmacology. Here are some intriguing aspects of this compound:
- Chemical Structure: This compound features a unique structure where a carbamate group is connected to an amino group, which is further substituted by a phenylethyl moiety. This structural configuration plays a significant role in its biological activity.
- Biological Relevance: Ethyl N-(1-phenylethylamino)carbamate has been studied for its potential applications in pharmacology. It may exhibit properties that are beneficial in medicinal chemistry, particularly in developing new therapeutic agents.
- Versatile Reactions: As a carbamate derivative, it can participate in a variety of chemical transformations, which makes it a valuable intermediate for synthesizing other complex organic molecules.
- Catalyst for Innovation: The compound serves as a promising candidate for drug discovery, especially due to its ability to mimic amino acids and influence biological pathways.
- Research Insights: Recent studies have explored its effects on neurotransmitter systems, hinting at its potential role in modulating mood and cognitive functions, although more research is needed to fully understand these mechanisms.
In conclusion, Ethyl N-(1-phenylethylamino)carbamate not only showcases the complexity of organic synthesis but also highlights the role of carbamate derivatives in the development of medicinal chemistry. As researchers continue to explore this compound, its contributions to science and potential therapeutic uses may unfold further.