Interesting facts
Interesting Facts about Ethyl N-(4-chlorophenyl)carbamate
Ethyl N-(4-chlorophenyl)carbamate, a member of the carbamate family, presents a fascinating blend of chemical properties and applications that make it a topic of interest in both academic and industrial settings. Here are some noteworthy facts about this compound:
- Biological Activity: This compound has been studied for its potential use in agricultural applications, particularly as a pesticide. Its ability to impact the nervous system of pests makes it a valuable candidate for crop protection.
- Pharmaceutical Relevance: Ethyl N-(4-chlorophenyl)carbamate has garnered attention in the pharmaceutical industry due to its structural similarities with various biologically active molecules, hinting at its potential as a lead compound for drug development.
- Synthetic Pathways: The synthesis of this compound can involve various strategies, including the reaction of 4-chlorophenol with ethyl carbamate. Understanding these synthesis methods helps chemists refine reaction conditions for yield optimization.
- Environmental Considerations: As with many synthetic chemicals, researchers are investigating the environmental impact of carbamate-based compounds. They aim to ensure that their use does not adversely affect non-target species or lead to bioaccumulation.
- Mechanism of Action: The study of how ethyl N-(4-chlorophenyl)carbamate interacts with biological systems can provide insights into its effectiveness and safety, paving the way for more targeted use in applications.
In summary, ethyl N-(4-chlorophenyl)carbamate stands out not only for its chemical properties but also for the broad scope of research surrounding its application and impact. As scientists continue to explore its potentials and limitations, this compound promises to remain a significant subject in chemical and environmental studies.
Synonyms
Ethyl 4-chlorophenylcarbamate
Carbamic acid, N-(4-chlorophenyl)-, ethyl ester
654-526-6
2621-80-9
Ethyl N-(4-chlorophenyl)carbamate
N-(P-Chlorophenyl)Urethane
Ethyl (4-chlorophenyl)carbamate
4-Chlorophenylurethane
p-Chlorophenylurethane
Ethyl p-chlorocarbanilate
Ethyl 4-chlorocarbanilate
N-(4-Chlorophenyl)ethylurethane
Ethyl N-(p-chlorophenyl)carbamate
p-Chlorocarbanilic acid ethyl ester
Ethyl (p-chlorophenyl)carbamate
Ethyl-N-(p-chlorophenyl)carbamate
NSC 26960
Carbamic acid, (4-chlorophenyl)-, ethyl ester
CARBANILIC ACID, p-CHLORO-, ETHYL ESTER
p-Chlorophenyl-urethane
BRN 0779335
AI3-51956
Carbamic acid, p-chlorophenyl-, ethyl ester
MFCD00018570
WLN: GR DMVO2
SCHEMBL1187952
DTXSID00180851
HMS1783A22
ethyl-N-(4-chlorophenyl)-carbamate
NSC26960
NSC-26960
AKOS001022204
4-Chlorophenylamine, N-ethoxycarbonyl-
(4-Chlorophenyl)carbamic acid ethyl ester
(4-Chlorophenyl)carbamic acid, Ethyl ester
DB-046898
ETHYL N-(PARA-CHLOROPHENYL)CARBAMATE
CS-0320578
N-(4-chlorophenyl)-carbamic acid ethyl ester
Carbamic acid, (p-chlorophenyl)-, ethyl ester
Q63395664
Z31707041
CARBAMIC ACID,N-(4-CHLOROPHENYL)-, ETHYL ESTER
Solubility of Ethyl N-(4-chlorophenyl)carbamate
Ethyl N-(4-chlorophenyl)carbamate, a carbamate compound, exhibits some interesting solubility characteristics. Understanding its solubility behavior is essential for various applications, including formulation chemistry and toxicological assessments. Here are a few key points regarding its solubility:
ethanol, acetone, or chloroform.
In conclusion, while ethyl N-(4-chlorophenyl)carbamate is not highly soluble in water, its dissolvability in organic solvents and dependency on environmental factors significantly broadens its applicability in chemical processes. Understanding these solubility traits is crucial for optimizing its use in various industrial and research applications.