Carbaryl

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Identification

Molecular formula
C12H11NO2
CAS Number
63-25-2
IUPAC Name
[3-(diethylamino)phenyl] N-methylcarbamate
Molecular Weight
201.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2330g/cm3
Synonyms
2631-26-7
Interesting facts

Interesting Facts about [3-(diethylamino)phenyl] N-methylcarbamate

[3-(diethylamino)phenyl] N-methylcarbamate is an intriguing compound with various applications in the field of chemistry and beyond. Here are some engaging insights:

  • Pharmaceutical Relevance: This compound belongs to a class of chemicals that are often used as intermediates in the synthesis of pharmaceuticals. Its unique structure makes it a valuable precursor for creating biologically active molecules.
  • Structure-Activity Relationship: The presence of the diethylamino group in its molecular framework allows for enhanced interaction with biological targets. Understanding how variations in the structure influence activity is a key element of medicinal chemistry.
  • Environmental Impact: Compounds like this one are studied for their degradability and impact on environmental health, making them significant in the domain of green chemistry. Researchers are continuously working to mitigate the ecological footprint of such substances.
  • Mechanism of Action: As a carbamate derivative, it may act as an inhibitor of certain enzymes, possibly impacting neurotransmitter activity. This is a common property seen in several carbamate-containing pesticides and drugs.
  • Popular Among Researchers: Due to its distinctive functional groups, [3-(diethylamino)phenyl] N-methylcarbamate is a subject of interest in multiple fields including organic synthesis, agrochemicals, and pharmaceutical research.

In summary, [3-(diethylamino)phenyl] N-methylcarbamate is more than just a chemical formula; it represents a fascinating intersection of theory and application in science. As researchers continue to uncover its potential, the implications for medicine and environmental science remain exciting.

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