Skip to main content

Etomidate

ADVERTISEMENT
Identification
Molecular formula
C11H18ClNO2
CAS number
15307-79-6
IUPAC name
2-(1-piperidyl)ethyl N-(4-chlorophenyl)carbamate
State
State

At room temperature, etomidate is typically in the form of a solid. Its crystalline structure allows it to maintain a stable form when stored properly.

Melting point (Celsius)
74.00
Melting point (Kelvin)
347.20
Boiling point (Celsius)
328.40
Boiling point (Kelvin)
601.60
General information
Molecular weight
244.73g/mol
Molar mass
244.7260g/mol
Density
1.2200g/cm3
Appearence

Etomidate appears as a white to almost white crystalline powder. It is odorless and has a slightly bitter taste.

Comment on solubility

Solubility of 2-(1-piperidyl)ethyl N-(4-chlorophenyl)carbamate

The solubility of 2-(1-piperidyl)ethyl N-(4-chlorophenyl)carbamate can significantly influence its behavior in various applications, particularly in pharmacology and biochemistry. Understanding its solubility properties is essential for effective formulation and dosing.

Key points regarding the solubility of this compound include:

  • Solvent Compatibility: This compound may exhibit varying solubility in polar and non-polar solvents, which can affect its bioavailability.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature. This relationship can be crucial for processes involving heat, such as synthesis.
  • pH Sensitivity: The solubility might be pH-dependent, given the presence of nitrogen functional groups that can be protonated.
  • Crystalline Form: Different polymorphs can possess distinct solubility characteristics, influencing its stability and activity.

In summary, while 2-(1-piperidyl)ethyl N-(4-chlorophenyl)carbamate may potentially dissolve in various solvents, the specific conditions and environment play critical roles in determining its solubility. It is essential to consider these factors when preparing solutions or formulations involving this compound.

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.

Synonyms
CHEMBL49907
BDBM50058192
(4-Chloro-phenyl)-carbamic acid 2-piperidin-1-yl-ethyl ester