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- 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
Identification
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.