Interesting facts
Interesting Facts about [3-(methoxycarbonylamino)phenyl] N-ethylcarbamate
[3-(methoxycarbonylamino)phenyl] N-ethylcarbamate is a fascinating compound with a variety of applications in the field of chemistry and beyond. As a carbamate derivative, it offers unique properties that make it a subject of study in various scientific domains.
Key Features:
- Biological Activity: This compound has been investigated for its potential biological activities, particularly in the realm of pharmaceuticals. Its structure suggests that it may interact with biological molecules effectively.
- Synthetic Utility: Due to the presence of both an amine and a carbamate functional group, [3-(methoxycarbonylamino)phenyl] N-ethylcarbamate serves as a versatile intermediate in organic synthesis. Chemists can use it to develop other important compounds.
- Research Relevance: Studies involving carbamate compounds like this one have expanded our understanding of enzyme inhibition and the development of herbicides, pesticides, and other agrochemicals. This makes such compounds particularly relevant in agricultural chemistry.
Considerations in Research:
When working with [3-(methoxycarbonylamino)phenyl] N-ethylcarbamate, researchers must consider:
- Toxicity and Safety: Like many carbamates, this compound may pose toxicity risks, particularly if used improperly. Comprehensive safety assessments are vital in laboratory settings.
- Environmental Impact: Understanding the environmental behavior of agrochemicals derived from this compound is crucial for sustainable agricultural practices.
In conclusion, [3-(methoxycarbonylamino)phenyl] N-ethylcarbamate is more than just a molecule; it represents the intersection of chemistry with pharmaceuticals and agriculture while offering insights into the complexity of biochemical interactions. Its ongoing study can contribute to advancements in multiple fields.
Synonyms
13684-83-8
CARBANILIC ACID, m-HYDROXY-, METHYL ESTER, ETHYLCARBAMATE (ester)
[3-(methoxycarbonylamino)phenyl] N-ethylcarbamate
P1GUI1BWD3
NSC-222531
Methyl m-hydroxycarbanilyl ethylcarbamate
NSC 222531
WLN: 2MVOR CMVO1
BRN 2419198
Methyl m-hydroxycarbanilate, ethylcarbamate
Carbanilic acid, m-hydroxy-, methyl ester, ethylcarbamate
Methyl m-hydroxycarbanilate ethylcarbamate
UNII-P1GUI1BWD3
DTXSID50159976
NSC222531
Carbanilic acid, methyl ester, ethylcarbamate
[3-(Methoxycarbonylamino)phenyl]n-ethylcarbamate
Carbanilic acid, methyl ester, ethylcarbamate (ester)
CARBAMIC ACID, ETHYL-, ESTER WITH METHYL M-HYDROXYCARBANILATE
Solubility of [3-(methoxycarbonylamino)phenyl] N-ethylcarbamate
[3-(methoxycarbonylamino)phenyl] N-ethylcarbamate exhibits notable solubility characteristics that can be influenced by several factors:
It is often described that solubility is a key factor in determining the compound's reactivity and bioavailability. As a general guideline, one might say, "Like dissolves like," indicating that the solubility of [3-(methoxycarbonylamino)phenyl] N-ethylcarbamate will be enhanced in solvents with similar polar character. Thus, understanding the solubility profile of this compound is essential for its effective application in various chemical processes.