Phenindamine

ADVERTISEMENT

Identification

Molecular formula
C24H27ClN2O
CAS Number
82-88-2
IUPAC Name
diethyl-[2-[4-(2-phenyl-1H-indol-3-yl)phenoxy]ethyl]ammonium;chloride
Molecular Weight
338.89g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1560g/cm3
Interesting facts

Interesting Facts about Diethyl-[2-[4-(2-phenyl-1H-indol-3-yl)phenoxy]ethyl]ammonium Chloride

Diethyl-[2-[4-(2-phenyl-1H-indol-3-yl)phenoxy]ethyl]ammonium chloride is a fascinating compound that showcases the intricate interplay between structure and function within chemical compounds. Here are some noteworthy points about this compound:

  • Versatile Uses: This compound belongs to the class of ammonium salts and is often explored for its potential applications in drug development and pharmaceutical sciences.
  • Indole Derivative: At the heart of this compound is a phenyl-indole moiety, which is well-known for its presence in many biologically active molecules. Indoles have garnered attention for various activities, including anti-cancer and anti-inflammatory properties.
  • Structure-Activity Relationship: The presence of the diethylammonium group at one end of the molecule contributes to its solubility and chemical reactivity, allowing scientists to investigate how structural tweaks can impact biological activity.
  • Receptor Targeting: The unique design of the compound may allow it to interact with specific biological receptors, making it a subject of interest in medicinal chemistry studies.
  • Research Significance: As a synthetic derivative, it can serve as a valuable tool in research aimed at understanding the pharmacodynamics of related compounds and their mechanisms of action.

This compound exemplifies the creativity inherent in the field of chemistry, where the exploration of complex structures can lead to significant advancements in therapeutic discoveries. As we delve deeper into its properties, the potential for novel applications continues to expand.

ADVERTISEMENT