Fenobucarb

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Identification

Molecular formula
C12H15NO2S
CAS Number
3766-81-2
IUPAC Name
(3-methyl-4-methylsulfanyl-phenyl) N-methylcarbamate
Molecular Weight
225.32g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1867g/cm3
Synonyms
3-Methyl-4-(methylthio)phenyl methylcarbamate
Interesting facts

Interesting Facts About (3-methyl-4-methylsulfanyl-phenyl) N-methylcarbamate

(3-methyl-4-methylsulfanyl-phenyl) N-methylcarbamate is a chemical compound that belongs to the category of carbamates, which are known for their diverse applications in various fields. Here are some engaging facts about this intriguing compound:

  • Historical Significance: Carbamates have been utilized since the mid-20th century and have played a crucial role in agricultural chemistry, particularly as pesticides and herbicides.
  • Mechanism of Action: Compounds in this class often work by inhibiting the enzyme acetylcholinesterase, which can disrupt nerve function in pests, making them effective in pest control.
  • Research Applications: Scientists are studying carbamates for their potential therapeutic uses, including the treatment of neurodegenerative diseases, due to their ability to influence neurotransmitter activity.
  • Environmental Impact: Understanding the environmental fate of carbamates like this one is essential. Their degradation products can sometimes be toxic, which underscores the importance of responsible usage and disposal.
  • Structural Intricacies: The unique structure of (3-methyl-4-methylsulfanyl-phenyl) N-methylcarbamate, with its specific substitutions, offers chemists insights into how variations in molecular structure can influence biological activity.

In summary, (3-methyl-4-methylsulfanyl-phenyl) N-methylcarbamate represents more than just a chemical formula; it embodies a blend of historical significance, ecological considerations, and cutting-edge research potential that continues to inspire chemists and environmental scientists alike.

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