Diethylcarbamazine
- Molecular formula
- C10H21N2O
- CAS Number
- 90-89-1
- IUPAC Name
- 2-(diethylamino)ethyl N-phenylcarbamate
- Molecular Weight
- 240.34g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0064g/cm3
- Synonyms
- 2-(diethylamino)ethyl N-phenylcarbamate
Identification
Interesting Facts about 2-(diethylamino)ethyl N-phenylcarbamate
The compound known as 2-(diethylamino)ethyl N-phenylcarbamate is a fascinating chemical with a variety of applications and implications in different fields.
Key Highlights
- Biological Activity: This compound exhibits interesting biological activity, making it a topic of interest in medicinal chemistry and pharmacology.
- Mechanism of Action: Its structure allows it to interact with biological systems in specific ways, potentially influencing enzyme activities or neurotransmitter pathways.
- Use in Research: Researchers often utilize this compound in studies related to drug development, particularly in exploring mechanisms of action for neurological disorders.
- Safety and Toxicology: Like many nitrogen-containing compounds, understanding the safety profile and potential toxicity is crucial for applications in pharmaceuticals.
As noted by many scientists in the field, “The key to advancing pharmacological studies lies in gaining a deeper understanding of compounds like 2-(diethylamino)ethyl N-phenylcarbamate.” This statement emphasizes the importance of such compounds in the continual search for new therapeutics.
Applications
- As an intermediate in synthesizing novel pharmaceutical agents.
- In the study of enzyme inhibition, especially in choline acetyltransferase research.
- Potential role in the development of pesticides due to its carbamate structure.
In summary, the exploration of 2-(diethylamino)ethyl N-phenylcarbamate helps unravel new biochemical pathways and fosters innovation in pharmaceutical sciences. Its intriguing properties make it a compound worth studying for anyone keen on the intersections of chemistry and biology.