Diethylaminoethanol hydrochloride

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Identification

Molecular formula
C8H20ClNO
CAS Number
300-92-5
IUPAC Name
[2-(3-benzyloxyanilino)-2-oxo-ethyl]-diethyl-ammonium;chloride
Molecular Weight
191.70g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0574g/cm3
Synonyms
19514-90-0
Interesting facts

Interesting Facts about [2-(3-Benzyloxyanilino)-2-Oxo-Ethyl]-Diethyl-Ammonium Chloride

This compound, with its complex structure, is a fascinating example of modern chemistry that blends organic synthesis with medicinal applications. Here are some interesting aspects to consider:

  • Synthetic Versatility: As a quaternary ammonium compound, it plays a pivotal role in various organic reactions, showcasing the versatility of ammonium salts in synthesis.
  • Potential Pharmacological Applications: Compounds of this nature often exhibit biological activity, making them of interest in pharmaceutical research. Their unique structures allow them to interact with biological membranes, possibly influencing drug delivery systems.
  • Research Interest: Due to the presence of the benzyloxy group, this compound is a subject of study for its potential as a *protective group* in organic reactions, illustrating its dual role in both structural and functional chemistry.
  • Importance of Functional Groups: The combination of the diethylammonium and the oxo-ethyl functional groups indicates potential properties that might be exploited in therapies concerning cell membranes or receptor binding.

To quote the famous chemist Linus Pauling, “Science is the search for truth.” In this case, the quest for understanding how compounds like [2-(3-Benzyloxyanilino)-2-Oxo-Ethyl]-Diethyl-Ammonium Chloride interact at the molecular level is a testament to the ongoing journey in chemical research.

In summary, this compound exemplifies how the interplay of various functional groups can lead to innovative uses in science and medicine. Continued exploration may yield exciting discoveries about its properties and potential applications.

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