Interesting facts
Interesting Facts About Ethyl N-[(ethoxycarbonylamino)methyl]carbamate
Ethyl N-[(ethoxycarbonylamino)methyl]carbamate is a fascinating compound within the realm of organic chemistry, particularly known for its unique structural features and diverse applications. Here are some intriguing insights regarding this compound:
- Functional Groups: This compound features several important functional groups, including a carbamate moiety, which is significant in medicinal chemistry for its role as a bioisostere in drug design.
- Applications: It finds utility in various sectors, including pharmaceuticals, where it serves as a precursor for different bioactive molecules.
- Biological Activity: Research has shown that derivatives of carbamate compounds can exhibit antifungal, antibacterial, and anti-inflammatory properties, making them critical targets in drug discovery.
- Reactivity: The presence of the ethoxycarbonyl group can enhance the reactivity of the compound, enabling chemists to perform further transformations efficiently.
- Synthesis: Understanding the synthetic pathways to produce ethyl N-[(ethoxycarbonylamino)methyl]carbamate can provide insights into more complex organic syntheses and improve yield and purity outcomes.
In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." Ethyl N-[(ethoxycarbonylamino)methyl]carbamate is a testament to this philosophy, serving as a platform for numerous innovative applications and a starting point for countless chemical explorations.
Overall, this compound is not just a simple structure; it exemplifies the intricacies of organic chemistry and the potential that such compounds hold in advancing modern science.
Synonyms
Methylene diurethane
3693-53-6
Diethyl methylenedicarbamate
Methylenediurethane
Methylene diurethan
Methylene bisurethane
Diethyl methylenebiscarbamate
Bis(N-ethoxycarbonylamino)methane
Carbamic acid, methylenebis-, diethyl ester
NSC 20524
CARBAMIC ACID, METHYLENEDI-, DIETHYL ESTER
ethyl N-[(ethoxycarbonylamino)methyl]carbamate
N,N'-Methylenebis-(ethyl carbamate)
V6BB652P9Y
N,N-Methylenebis(ethyl carbamate)
NSC-20524
N,N-Methylene-bis(ethyl carbamate)
EINECS 223-011-4
BRN 1812852
Methylendiurethan
UNII-V6BB652P9Y
WLN: 20VM1MVO2
Carbamic acid, methylenebis-, diethyl ester (9CI)
diethyl methanediylbiscarbamate
SCHEMBL7618800
DTXSID50190420
N,N'-Methylenebis(ethyl carbamate)
NSC20524
STL290400
AKOS001026961
AS-86917
C,C'-Diethyl N,N'-methylenebis[carbamate]
DB-255302
CS-0332560
NS00030127
G92351
Z56756237
Carbamic acid, N,N'-methylenebis-, C,C'-diethyl ester
Solubility of Ethyl N-[(ethoxycarbonylamino)methyl]carbamate
The solubility of ethyl N-[(ethoxycarbonylamino)methyl]carbamate can be influenced by various factors, including temperature, pH, and the nature of the solvent used. This compound, being an organocarbamate, typically exhibits the following solubility characteristics:
In summary, while ethyl N-[(ethoxycarbonylamino)methyl]carbamate may exhibit some solubility in aqueous environments, it is essential to consider the factors listed above to fully understand its solubility behavior. As always, experimental conditions may yield specific results that differ from general predictions.