Interesting facts
Exploring Ethyl N-Hydroxycarbamate
Ethyl N-hydroxycarbamate is a fascinating chemical compound that holds significance in various fields, particularly in organic synthesis and medicinal chemistry. Here are some intriguing facts about this compound:
- Functional Group Features: This compound features a hydroxy group (-OH) attached to a carbamate, which is known for its reactivity and importance in forming amine derivatives.
- Biological Relevance: Ethyl N-hydroxycarbamate has been studied for its potential role in biological systems, particularly in the context of drug metabolism and detoxification.
- Synthetic Utility: The unique structure of ethyl N-hydroxycarbamate makes it a valuable intermediate in the preparation of other complex organic molecules, showcasing its versatility in synthetic routes.
- Research Applications: Researchers have explored its application in the development of pharmaceuticals, particularly in the synthesis of anti-cancer agents and other therapeutic compounds.
- Toxicology Studies: Understanding the safety profile of ethyl N-hydroxycarbamate is crucial, as some derivatives have been investigated for their potential toxic effects, further emphasizing the importance of safety in chemical research.
As a compound at the intersection of organic chemistry and pharmacology, ethyl N-hydroxycarbamate exemplifies the intricate relationships within chemical structures and their potential applications. The ongoing research into this compound can lead to breakthroughs in understanding drug interactions and effects on human health.
Synonyms
N-Hydroxyurethane
Ethyl hydroxycarbamate
Ethyl N-hydroxycarbamate
Hydroxyurethane
N-Hydroxyurethan
Hydroxyurethan
N-Hydroxy ethyl carbamate
CARBAMIC ACID, HYDROXY-, ETHYL ESTER
Ethyl-N-hydroxycarbamate
N-Hydroxyethyl carbamate
SQ 16819
CCRIS 342
QWI3C4ASI7
EINECS 209-648-0
Ethylester kyseliny N-hydroxykarbaminove
BRN 1747529
AI3-52582
UNII-QWI3C4ASI7
Ethylester kyseliny N-hydroxykarbaminove [Czech]
CCRIS-342
VGEWEGHHYWGXGG-UHFFFAOYSA-
DTXSID20207635
4-03-00-00168 (Beilstein Handbook Reference)
SQ-16819
DTXCID70130126
inchi=1/c3h7no3/c1-2-7-3(5)4-6/h6h,2h2,1h3,(h,4,5)
vgeweghhywgxgg-uhfffaoysa-n
589-41-3
Hydroxycarbamic acid ethyl ester
N-Carbethoxyhydroxylamine
NSC-71045
NSC-83629
MFCD00002108
CHEMBL153081
NHU
Carbamic acid, N-hydroxy-, ethyl ester
WLN: QMVO2
ethylhydroxycarbamate
Ethyl hydroxycarbamate #
N-carboethoxyhydroxylamine
N-ethoxycarbonylhydroxylamine
SCHEMBL36772
SCHEMBL11678696
NSC71045
NSC83629
BDBM50121952
AKOS015856775
AS-40148
SY051112
CS-0235105
H0618
NS00034046
EN300-152827
N-Carbethoxyhydroxylamine, Ethyl N-hydroxycarbamate, Hydroxycarbamic acid ethyl ester
Solubility of Ethyl N-Hydroxycarbamate
Ethyl N-hydroxycarbamate, with the chemical formula C3H7NO3, displays interesting solubility characteristics which are significant in various chemical processes. Here are key points to consider:
The effective solubility of ethyl N-hydroxycarbamate not only facilitates its use in laboratory settings but also underscores its relevance in manufacturing processes. As with many compounds, the balance of polar and non-polar characteristics plays a crucial role in determining its solubility profile.