Fenobucarb
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- 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
Identification
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.