Carbaryl

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Identification

Molecular formula
C12H11NO2
CAS Number
63-25-2
IUPAC Name
2-(1-piperidyl)ethyl N-(2,6-dichloro-4-pentoxy-phenyl)carbamate
Molecular Weight
201.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2500g/cm3
Synonyms
K 924
Interesting facts

Exploring 2-(1-piperidyl)ethyl N-(2,6-dichloro-4-pentoxy-phenyl)carbamate

This intriguing compound, known as a carbamate, is notable for its potential applications in various fields, particularly in medicinal chemistry and agriculture. Here are some fascinating aspects to consider:

  • Structural Complexity: The presence of a piperidine ring in its structure provides unique properties that influence its interactions with biological systems.
  • Biological Activity: Carbamates are known for their ability to inhibit certain enzymes, making this compound a topic of interest in drug development, especially in treating neurological disorders.
  • Versatile Applications: Beyond pharmacology, it has potential uses in agriculture, functioning as a pesticide or herbicide due to its chemical stability.
  • Halogen Influence: The incorporation of chlorine atoms in its molecular structure enhances its biological activity and also may increase lipophilicity, affecting how the compound interacts with cell membranes.
  • Safety Considerations: As with many chemical compounds, understanding the safety profile is critical, especially considering its applications in pesticides and the potential environmental impact.

This compound exemplifies the intersection of chemistry and application, showcasing how structural variations can lead to diverse functionalities. The study of such compounds not only enhances our understanding of chemical interactions but also opens pathways for innovation in drug design and agricultural practices.

As noted by chemists, “The design of a compound often determines its destiny.” This highlights the importance of structural analysis in predicting the behavior and utility of chemical substances.

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