Propoxur

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Identification

Molecular formula
C11H15NO3
CAS Number
114-26-1
IUPAC Name
(2-isopropylphenyl) N-methylcarbamate
Molecular Weight
209.24g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0460g/cm3
Synonyms
Isoprocarb
Interesting facts

Interesting Facts about (2-isopropylphenyl) N-methylcarbamate

(2-isopropylphenyl) N-methylcarbamate is a fascinating compound with applications that reflect its unique chemical structure and properties. Here are some noteworthy facts:

  • Applications in Agriculture: This compound is often used as a pesticide. It showcases the vital role of carbamate derivatives in protecting crops from pests while being less toxic to humans and wildlife compared to other pesticide classes.
  • Mechanism of Action: As a carbamate, it works by inhibiting the enzyme acetylcholinesterase, which plays a crucial role in neurotransmission. By blocking this enzyme, it disrupts the normal function of neurotransmitters, leading to pest mortality.
  • Structurally Unique: The presence of the 2-isopropylphenyl group contributes to the compound's lipophilicity, allowing it to penetrate biological membranes effectively. This structural characteristic impacts its overall efficacy and pharmacokinetics.
  • Sustainability Considerations: As the agricultural sector moves toward more sustainable practices, compounds like (2-isopropylphenyl) N-methylcarbamate are being scrutinized for environmental impact. Research continues to optimize its use while minimizing ecological risks.
  • Regulatory Status: Like many pesticides, (2-isopropylphenyl) N-methylcarbamate is subjected to rigorous evaluation by regulatory agencies. This ensures it meets safety standards and efficacy before being approved for various agricultural applications.

In summary, (2-isopropylphenyl) N-methylcarbamate stands as an example of the intricate relationship between chemical structure and biological function, highlighting the ongoing evolution of chemistry in addressing modern agricultural challenges.

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