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.
Synonyms
3-Methyl-4-(methylthio)phenyl methylcarbamate
BAY 32651
3566-00-5
4-(Methylthio)-m-tolyl methylcarbamate
BAY S 2758
DRC 1325
3-Methyl-4-methylthiophenyl N-methylcarbamate
ENT 25,777
5RAJ4I7CLF
SK 79
NSC 107927
BRN 1970900
Phenol, 3-methyl-4-(methylthio)-, methylcarbamate
AI3-25777
3-Methyl-4-(methylthio)phenol methylcarbamate
UNII-5RAJ4I7CLF
BAY-32651
NSC-107927
Carbamic acid, methyl-, 4-methylthio-m-tolyl ester
Carbamic acid, methyl-, 3-methyl-4-(methylthio)phenyl ester
DTXSID5041485
BAYER-32651
BAY-S-2758
SK-79
Carbamic acid, methyl-, 4-(methylthio)-m-tolyl ester
4-METHYLTHIO-(3-METHYLPHENYL)-N-METHYLCARBAMATE
PHENOL, 3-METHYL-4-(METHYLTHIO)-, 1-(N-METHYLCARBAMATE)
3-methyl-4-(methylsulfanyl)phenyl N-methylcarbamate
DTXCID3021485
4-(methylthio)-m-Tolyl methylcarbamic acid
Phenol, 3-methyl-4-(methylthio)-, methylcarbamate (9CI)
Bayer 32651
WLN: 1SR B1 DOVM1
SCHEMBL9391203
CHEMBL2288487
NSC107927
AKOS024337014
Carbamic acid, 4-(methylthio)-m-tolyl ester
NS00022090
Solubility of (3-methyl-4-methylsulfanyl-phenyl) N-methylcarbamate
The solubility of (3-methyl-4-methylsulfanyl-phenyl) N-methylcarbamate is an intriguing characteristic that can impact its behavior in various chemical environments. Understanding the solubility of this compound is essential for its applications and interactions. Here are several key points regarding its solubility:
In conclusion, while the solubility profile of (3-methyl-4-methylsulfanyl-phenyl) N-methylcarbamate is influenced by various factors, it is essential to conduct empirical tests to fully characterize its solubility characteristics. As the saying goes, "A compound is only as soluble as its environment."