Carbaryl

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Identification

Molecular formula
C12H11NO2
CAS Number
63-25-2
IUPAC Name
(4-aminophenyl) N-methylcarbamate
Molecular Weight
201.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2300g/cm3
Synonyms
Methylcarbamic acid 4-aminophenyl ester
Interesting facts

Interesting Facts about (4-aminophenyl) N-methylcarbamate

(4-aminophenyl) N-methylcarbamate, often referred to in the scientific community as a derivative of carbamate, combines the amine functionality with a carbamate structure. This compound is noteworthy for several reasons:

  • Biological Activity: The primary significance of (4-aminophenyl) N-methylcarbamate lies in its potential biological activities. It has been studied for its effects on acetylcholinesterase, an enzyme critical for neurotransmitter regulation.
  • Pesticide Development: Compounds in the carbamate family, including this one, are frequently utilized in the development of pesticides due to their ability to inhibit cholinesterase, leading to increased effectiveness in pest control.
  • Synthesis Roadmap: The synthesis of (4-aminophenyl) N-methylcarbamate can involve several chemical transformations, making it an excellent subject for students learning about organic synthesis pathways. The typical steps include aminolysis and carbamoylation.
  • Research Potential: Ongoing research indicates that compounds like this one could pave the way for novel therapeutics in treating conditions associated with neurotransmitter dysregulation.

As with all chemical entities, proper handling and understanding of its properties are crucial. Research into (4-aminophenyl) N-methylcarbamate not only broadens our knowledge of organic chemistry but also highlights the importance of such compounds in practical applications.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This encapsulates the spirit of exploring compounds like (4-aminophenyl) N-methylcarbamate, urging scientists to delve deeper into its potential!

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