Interesting facts
Interesting Facts about Ethyl N-phenylcarbamate
Ethyl N-phenylcarbamate is a fascinating compound with diverse applications and intriguing properties. Here are several notable facts that highlight its significance:
- Chemical Family: Ethyl N-phenylcarbamate belongs to the class of carbamate compounds, which are esters or salts derived from carbamic acid. These types of compounds are widely recognized for their roles in both natural and synthetic environments.
- Pesticide Efficacy: This compound has been studied for its potential use as an agricultural pesticide. Its structure allows it to interact with biological systems, making it effective against a variety of pests while providing a degree of selectivity that minimizes harm to beneficial species.
- Pharmaceutical Applications: Ethyl N-phenylcarbamate has garnered attention in pharmaceutical research for its potential as an analgesic or anti-inflammatory agent. Investigating its effects on biological activity continues to be an area of interest among scientists.
- Mechanism of Action: Compounds in the carbamate class are known to inhibit acetylcholinesterase, an enzyme critical for neurotransmitter regulation. This mechanism suggests that ethyl N-phenylcarbamate could influence nerve signal transmission, valuable for exploring therapeutic pathways.
- Synthetic Pathways: The synthesis of ethyl N-phenylcarbamate typically involves the reaction of phenyl isocyanate with ethyl alcohol. This straightforward method highlights the importance of isocyanates in the production of various carbamate derivatives.
As with many chemical compounds, understanding the properties and potential applications of ethyl N-phenylcarbamate opens new avenues for research and development in medicinal chemistry and agricultural science.
In summary, this compound demonstrates a rich interplay between chemistry and practical applications, underscoring the importance of carbamate compounds in everyday life.
Synonyms
101-99-5
Phenylurethane
N-Phenylurethane
ETHYL N-PHENYLCARBAMATE
Ethyl phenylcarbamate
Phenylurethan
Ethyl carbanilate
Euphorin
Keimstop
Carbamic acid, N-phenyl-, ethyl ester
Urethane, phenyl-
Carbanilic acid, ethyl ester
Phenylethyl carbamate
Ethyl N-phenylurethan
Carbamic acid, phenyl-, ethyl ester
Ethyl N-phenylurethane
Phenylurethan(e)
Urethan, phenyl-
N-(Ethoxycarbonyl)aniline
EPC (the plant regulator)
Ethyl-N-phenylcarbamate
Ethanol, carbanilate
N-PHENYLETHYL CARBAMATE
N-Phenyl ethylcarbamate
HSDB 5344
UNII-TWP7W286IF
NSC 3245
EINECS 202-995-9
ethylphenylcarbamate
Ethylester kyseliny karbanilove
BRN 1942785
AI3-15353
NSC-3245
Ethyl N-phenylcarbanilate
PHENYLURETHANE [MI]
TWP7W286IF
DTXSID0059243
LBKPGNUOUPTQKA-UHFFFAOYSA-
Ethyl ester of phenylcarbamic acid
N-Phenylcarbamic Acid Ethyl Ester
4-12-00-00619 (Beilstein Handbook Reference)
ETHYL N-PHENYLCARBAMATE [HSDB]
Epc(the plant regulator)
Ethylester kyseliny karbanilove [Czech]
NPhenylurethane
ethylcarbanilate
phenyl urethane
EUPHORIN(Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 652)
EUPHORIN[Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 652]
KEIMSTOP(Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 652)
KEIMSTOP[Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 652]
Ethyl Nphenylurethan
Ethyl Nphenylurethane
MFCD00026806
URETHAN, PHENYL
URETHANE, PHENYL
N(Ethoxycarbonyl)aniline
WLN: 2OVMR
SCHEMBL264865
Phenylcarbamic acid ethyl ester
CHEMBL2235373
DTXCID3032593
NSC3245
N-phenyl carbamic acid ethyl ester
N-phenyl-carbamic acid ethyl ester
N-phenyl-carbamic acid-ethyl ester
Carbamic acid, phenyl, ethyl ester
STK369865
AKOS002937614
NCGC00342033-01
AS-63172
CS-0312803
NS00023097
P0165
E78800
AB00375764-03
Q3742461
Solubility of Ethyl N-phenylcarbamate
Ethyl N-phenylcarbamate, commonly referred to in chemical literature, exhibits some interesting solubility characteristics that are worth noting. This compound possesses properties that can affect its interaction with various solvents:
In summary, one can observe that the solubility of ethyl N-phenylcarbamate is predominantly influenced by:
Understanding these aspects of solubility is crucial for applications in various chemical processes, such as synthesis and extraction. As such, testing the solubility in different environments may yield more specific insights into its behavior in practical applications.