Interesting facts
Intriguing Facts About (2-chlorophenyl) N-methylcarbamate
(2-chlorophenyl) N-methylcarbamate, commonly known as a carbamate compound, plays a vital role in both agricultural and pharmaceutical applications. Here are some fascinating insights about this intriguing compound:
- Versatile Applications: This compound is primarily used as a pesticide, known for its effectiveness in controlling pests in various crops.
- Mechanism of Action: Carbamates inhibit acetylcholinesterase, an enzyme crucial for the breakdown of acetylcholine, leading to an accumulation of this neurotransmitter. This mechanism results in enhanced nerve signaling, which can be lethal to pests.
- Research Interest: Chemists are studying the metabolism of (2-chlorophenyl) N-methylcarbamate to improve its efficiency and reduce potential environmental impacts, making it a subject of ongoing research in agrochemicals.
- Toxicity Considerations: While effective against pests, it's essential to handle this compound with care. Understanding its toxicity profile helps ensure safety for humans and non-target organisms.
- Structural Significance: The presence of the chlorophenyl group not only contributes to its pesticidal properties but also influences its interaction with biological systems, making the study of its structure-function relationship particularly interesting.
In summary, (2-chlorophenyl) N-methylcarbamate exemplifies the balance between agricultural efficiency and safety. As scientists continue to explore its applications and effects, it underscores the importance of responsible use and understanding of chemical compounds within our ecosystems.
Synonyms
Etrofol
2-Chlorophenyl methylcarbamate
3942-54-9
Hoppside
Hopcide
O-CHLOROPHENYL METHYLCARBAMATE
2-Chlorophenyl-N-methylcarbamate
Carbamic acid, methyl-, 2-chlorophenyl ester
2-chlorophenyl N-methylcarbamate
HSDB 2609
EINECS 223-524-3
Carbamic acid, methyl-, o-chlorophenyl ester
Ro 7-4780
BRN 2048887
R4I4K15V9B
AI3-27692
Carbamic acid, N-methyl-, 2-chlorophenyl ester
4-06-00-00795 (Beilstein Handbook Reference)
O-CHLOROPHENYL METHYLCARBAMATE [HSDB]
2ChlorophenylNmethylcarbamate
2Chlorophenyl methylcarbamate
oChlorophenyl Nmethylcarbamate
Ro 74780
Carbamic acid, methyl, 2chlorophenyl ester
Carbamic acid, methyl, ochlorophenyl ester
Carbamic acid, Nmethyl, 2chlorophenyl ester
223-524-3
CPMC
(2-chlorophenyl) N-methylcarbamate
o-Chlorophenyl N-methylcarbamate
UNII-R4I4K15V9B
SCHEMBL1525967
DTXSID3058084
AKOS006278982
1ST20621
DB-228033
NS00030574
Q27287784
Solubility of (2-chlorophenyl) N-methylcarbamate
(2-chlorophenyl) N-methylcarbamate is known for its unique solubility characteristics which can greatly influence its applications and behavior in different environments. Understanding the solubility of this compound is essential for predicting its reactivity and interaction with various solvents.
As we dive deeper into its solubility profile, it's crucial to remember that pH levels and the presence of other ions in solution can also impact solubility. Thus, the phrase “solubility is context-dependent” truly captures the essence of (2-chlorophenyl) N-methylcarbamate in varying environments.