Carbaryl

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Identification

Molecular formula
C12H11NO2
CAS Number
63-25-2
IUPAC Name
[3-(but-2-enoylamino)phenyl] N-methylcarbamate
Molecular Weight
201.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2300g/cm3
Interesting facts

Interesting Facts about [3-(but-2-enoylamino)phenyl] N-methylcarbamate

[3-(but-2-enoylamino)phenyl] N-methylcarbamate is a fascinating compound that belongs to the class of carbamates, which are widely recognized for their diverse biological activities. Here are some intriguing facts about this compound:

  • Biological Relevance: This compound may serve as an important building block in medicinal chemistry, particularly in the development of pharmaceuticals that target specific biological pathways.
  • Structural Versatility: The presence of the but-2-enoylamino group introduces interesting reactivity opportunities, allowing it to participate in various chemical reactions, including polymerization and conjugation reactions.
  • Enzyme Interaction: Carbamates are known for their ability to interact with various enzymes, including acetylcholinesterase, which plays a crucial role in neurotransmission. Studying this compound might provide insights into its potential inhibitory effects.
  • Synthetic Pathways: The synthesis of [3-(but-2-enoylamino)phenyl] N-methylcarbamate showcases an elegant intersection of organic synthesis techniques, highlighting the creativity and innovation required in modern chemistry.
  • Potential Applications: Researchers are exploring its potential use in agricultural chemistry as a pesticide or herbicide due to the inherent activity of carbamates in these applications.

As a compound that bridges various fields of chemistry, [3-(but-2-enoylamino)phenyl] N-methylcarbamate exemplifies the complexity and richness of chemical science. Its study can open pathways to new discoveries in drug design, agricultural solutions, and fundamental chemistry.

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