Interesting facts
Interesting Facts about Ethyl N-methylcarbamate
Ethyl N-methylcarbamate is a fascinating compound that is not only integral in various chemical applications but also has historical significance in the field of chemistry. Here are some captivating details about this compound:
- Versatile Usage: Ethyl N-methylcarbamate is commonly used in the synthesis of various pharmaceuticals and chemical intermediates, making it a valuable building block in medicinal chemistry.
- Pest Control Applications: This compound has been identified as useful in the formulation of pesticides due to its effectiveness against certain pests, thus contributing to agricultural advancements.
- Historical Context: The development of carbamate compounds, including ethyl N-methylcarbamate, traces back to the mid-20th century, marking an era where scientists began exploring more sustainable and less toxic alternatives for organophosphate pesticides.
- Mechanism of Action: Carbamates, in general, work by inhibiting the enzyme acetylcholinesterase, which plays a vital role in the nervous system, showcasing the intricate relationship between chemistry and biology.
- Research and Studies: Ongoing research continues to explore the implications of ethyl N-methylcarbamate in various fields, from environmental science to pharmacology, reinforcing its significance in contemporary studies.
In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." Ethyl N-methylcarbamate exemplifies how one compound can lead to numerous innovative applications and discoveries in science.
From its role in pharmaceuticals to its impact on agricultural practices, ethyl N-methylcarbamate highlights the importance of chemical compounds in shaping our world.
Synonyms
Ethyl methylcarbamate
N-Methylurethane
105-40-8
ETHYL N-METHYLCARBAMATE
N-Methylurethan
Ethyl-N-methylcarbamate
Carbamic acid, methyl-, ethyl ester
Methylcarbamic acid, ethyl ester
N-Methyl urethan
Methylurethane (VAN)
N-Methylcarbamic acid, ethyl ester
CCRIS 2510
HSDB 5367
CH3NHCOOC2H5
UNII-1W34GCF5CS
NSC 8836
EINECS 203-295-6
BRN 1743375
METHYL-CARBAMIC ACID ETHYL ESTER
AI3-09519
NSC-8836
Ethylester kyseliny methylkarbaminove
Carbamic acid, N-methyl-, ethyl ester
1W34GCF5CS
DTXSID2031746
4-04-00-00200 (Beilstein Handbook Reference)
ETHYL N-METHYLCARBAMATE [HSDB]
N-Methylcarbamic acid ethyl ester
NMethylurethan
NMethylurethane
methyl urethane
methyl-urethane
NMethyl urethan
Ethylester kyseliny methylkarbaminove [Czech]
EthylNmethylcarbamate
MFCD00041924
ethyl(methyl)carbamate
ethyl-n-methyl carbamate
WLN: 2OVM1
SCHEMBL42229
ETHYL METHYLAMINOFORMATE
methylcarbamic acid ethyl ester
NMethylcarbamic acid ethyl ester
CHEMBL1232511
DTXCID0011746
NSC8836
N-methyl-carbamic acid ethyl ester
Carbamic acid, methyl, ethyl ester
AKOS006221441
DB02856
NCI60_041953
CS-0187425
M0456
NS00023372
D91332
Q27093818
Solubility of Ethyl N-methylcarbamate
Ethyl N-methylcarbamate, with the chemical formula C4H9N1O2, displays unique solubility characteristics that are essential in understanding its applications and behavior in various environments.
Key Points on Solubility:
As a rule of thumb, "the solubility of a substance greatly depends on the nature of both the solute and the solvent." In the case of Ethyl N-methylcarbamate, its solubility profile allows it to be utilized effectively in various chemical processes, making it a compound of interest for further studies.