Dimethylaminoethyl diphenylcarbamate
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- Molecular formula
- C18H22N2O2
- CAS Number
- 538-91-2
- IUPAC Name
- 2-(dimethylamino)ethyl N,N-diphenylcarbamate
- Molecular Weight
- 312.39g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1010g/cm3
Identification
Interesting facts
Interesting Facts about 2-(Dimethylamino)ethyl N,N-Diphenylcarbamate
2-(Dimethylamino)ethyl N,N-diphenylcarbamate is an intriguing compound that finds a significant role in the field of organic chemistry and medicinal applications. Here are some noteworthy aspects of this compound:
- Biological Activity: This compound exhibits potential biological activity, making it a subject of interest in pharmacology. Its derivatives are explored for their effectiveness in various medicinal applications.
- Structure Diversity: The presence of a dimethylamino group and two phenyl rings contributes to the structural diversity of this compound. The electronic properties of these groups can influence its reactivity and interactions.
- Use as a Carbamate: As a carbamate derivative, it’s utilized in the synthesis of pesticides, herbicides, and various pharmaceuticals, showcasing its industrial relevance.
- Research Applications: Scientists have been investigating this compound for its potential as a catalyst in organic reactions, emphasizing its utility in synthetic chemistry.
- Safety Considerations: While exploring its properties, researchers pay close attention to the safety profiles of such compounds, as some carbamates can exhibit toxicity and environmental concerns.
As a specialized subject of study, 2-(dimethylamino)ethyl N,N-diphenylcarbamate serves as a reminder of the intricate connections between molecular structure and function. It highlights the continuous exploration within the realms of chemistry and potential therapeutic landscapes.