Neostigmine

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Identification

Molecular formula
C13H22N2O2
CAS Number
59-99-4
IUPAC Name
2-(diethylamino)ethyl N-(2-naphthyl)carbamate
Molecular Weight
303.36g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1400g/cm3
Synonyms
2-NAPHTHALENECARBAMIC ACID, 2-DIETHYLAMINOETHYL ESTER
Interesting facts

Interesting Facts About 2-(Diethylamino)ethyl N-(2-naphthyl)carbamate

2-(Diethylamino)ethyl N-(2-naphthyl)carbamate is a fascinating compound with a variety of applications in different scientific fields. Here are some insights that highlight its significance and unique properties:

  • Pharmaceutical Relevance: This compound contains a carbamate functional group, which is prevalent in many pharmaceuticals. Carbamates are known for their role as inhibitors in certain enzymatic processes, making them crucial in drug development.
  • Pesticide Applications: Due to its ability to interact with biological systems, this compound has potential applications in agriculture as a pesticide. Its efficacy in targeting specific pests without harming non-target species is an area of ongoing research.
  • Structure-Activity Relationship (SAR): The presence of both a diethylamino group and a naphthyl moiety allows scientists to explore how structural changes can influence biological activity, providing insights that aid the design of more effective compounds.
  • Analytical Chemistry: This compound serves as an intriguing subject for analytical chemists interested in developing methods for the synthesis and detection of carbamate derivatives. Its unique structure can help refine techniques such as chromatography and spectrometry.
  • "Molecular Versatility": The branching nature of its molecular structure allows for various modifications, potentially leading to new derivatives with tailored properties and activities. This versatility makes it a valuable compound in medicinal chemistry.

Overall, 2-(diethylamino)ethyl N-(2-naphthyl)carbamate embodies the intersection of organic synthesis, pharmacology, and analytical methods. Its diverse applications highlight not only its utility in practical fields but also the endless possibilities that arise from studying such complex chemical entities.

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