Etomidate hydrochloride

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Identification

Molecular formula
C14H18ClN3O2
CAS Number
135861-58-2
IUPAC Name
2-(3-ethoxycarbonyl-5-methoxy-2-methyl-indol-1-yl)ethyl-diethyl-ammonium;chloride
Molecular Weight
308.79g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1186g/cm3
Synonyms
Of-2439
Interesting facts

Interesting Facts about 2-(3-Ethoxycarbonyl-5-methoxy-2-methyl-indol-1-yl)ethyl-diethyl-ammonium; chloride

This intriguing compound is a member of the indole derivatives, which are a class of compounds known for their diverse biological activities. Here are some fascinating aspects about this compound:

  • Biological Significance: Indole derivatives have been extensively studied for their roles in medicinal chemistry, particularly for their potential anti-cancer, anti-inflammatory, and anti-oxidative properties.
  • Structure-Activity Relationship: The specific substitution patterns on the indole ring influence not only the biological activity of the compound but also its pharmacokinetic properties. For example, the ethoxycarbonyl and methoxy groups can enhance solubility and modulate binding affinity to biological targets.
  • Quaternary Ammonium Structure: As it contains a quaternary ammonium moiety, this compound can interact with biological membranes, which may allow for unique mechanisms of action in drug delivery systems.
  • Versatile Synthesis: Compounds like this can often be synthesized through multi-step reactions, showcasing the elegance and complexity of organic synthesis in generating targeted pharmacophores.
  • Potential in Drug Development: Due to its structural features, this compound represents a promising candidate for drug development, especially in the context of targeting specific biological pathways.

In summary, 2-(3-Ethoxycarbonyl-5-methoxy-2-methyl-indol-1-yl)ethyl-diethyl-ammonium; chloride exemplifies the intricate relationship between molecular structure and biological function, making it a valuable compound for further research in medicinal chemistry.

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