Etomidate

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Identification

Molecular formula
C11H18ClNO2
CAS Number
15307-79-6
IUPAC Name
2-(1-piperidyl)ethyl N-(4-chlorophenyl)carbamate
Molecular Weight
244.73g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2200g/cm3
Synonyms
CHEMBL49907
Interesting facts

Interesting Facts about 2-(1-Piperidyl)ethyl N-(4-chlorophenyl)carbamate

2-(1-Piperidyl)ethyl N-(4-chlorophenyl)carbamate, often referred to in scientific literature for its diverse biological activities, is an intriguing compound that has garnered significant interest in the fields of medicinal chemistry and pharmacology.

Key Highlights:

  • Versatile Applications: This compound acts as a potent carbamate derivative, widely utilized for its potential in developing therapeutic agents.
  • Mechanism of Action: Its structure facilitates interactions with enzyme systems in the body, influencing neurotransmitter activities and offering prospects for neurological disorders.
  • Research Potential: Scientists are actively investigating its efficacy as an antidepressant and its overall impact on mood regulation.
  • Chlorophenyl Influence: The presence of the 4-chlorophenyl moiety enhances its lipophilicity, making it a subject of interest in drug design, especially for delivering compounds across biological membranes.

Quote from the Field:

As noted by researchers, "The unique structural characteristics of carbamates like this compound open new avenues for the synthesis of innovative therapeutic agents."

In summary, 2-(1-piperidyl)ethyl N-(4-chlorophenyl)carbamate is not just a molecule; it is a window into the potential advancements in pharmacotherapy, bridging the gap between chemical structure and biological effectiveness.

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