Interesting facts
Fascinating Facts about 1-Chloro-2-ethylsulfanyl-ethane
1-Chloro-2-ethylsulfanyl-ethane, also known in the scientific community as a potential pharmaceutical intermediate, presents numerous intriguing aspects worth exploring. Here are some highlights:
- Structural Insights: This compound features a unique arrangement with a chlorine atom attached to the first carbon and an ethylsulfanyl group on the second carbon. Such configurations can influence the reactivity and stability of the molecule.
- Synthetic Utility: It serves as a valuable intermediate in organic synthesis. As an important building block, it aids in the formation of more complex organic compounds through various reactions such as nucleophilic substitution.
- Application Potential: The presence of both chlorine and sulfide functionalities opens up opportunities for the synthesis of biologically active molecules, potentially leading to the discovery of new pharmaceuticals.
- Reactivity: The chlorine atom can participate in nucleophilic substitution reactions, making it a keen target for various nucleophiles. This versatility is a significant characteristic for chemists working in drug development.
- Environmental Impact: Like many chlorinated compounds, there is an ongoing conversation in the scientific community regarding the environmental persistence of compounds like 1-chloro-2-ethylsulfanyl-ethane. Understanding its behavior and degradation pathways is essential for safety and regulatory assessments.
Conclusion
1-Chloro-2-ethylsulfanyl-ethane is a compound that embodies the intricate balance of chemical properties and practical applications. Its role in synthesis underscores the importance of chlorinated and sulfide compounds in the continuing journey of chemical research and development. As we delve deeper, the hope is to unlock its full potential and address any challenges it presents.
Synonyms
2-CHLOROETHYL ETHYL SULFIDE
693-07-2
1-Chloro-2-(ethylthio)ethane
2-Ethylthioethyl chloride
Ethane, 1-chloro-2-(ethylthio)-
Half-mustard gas
Sulfide, chloroethyl ethyl
Chlordiethylsulfid
2-Chloroethyl ethyl thioether
2-Chloroethyl(ethyl)sulfide
h-Mg; half-mustard gas
Chlorothiolalcohol (CTA)
Chlordiethylsulfid [Czech]
Sulfide, diethyl 2-chloro
Ethyl beta-chloroethyl sulfide
NSC 10977
HSDB 5744
1-Chloro-2-(ethylsulfanyl)ethane
EINECS 211-742-1
UNII-5MN267Q6RG
beta-Ethylmerkaptoethylchlorid
beta-Ethylmerkaptoethylchlorid [Czech]
BRN 0635672
.beta.-Ethylmerkaptoethylchlorid
DTXSID3027295
NSC-10977
DTXCID807295
Ethyl .beta.-chloroethyl sulfide
4-01-00-01407 (Beilstein Handbook Reference)
CHLOROETHYL(ETHYL)SULFIDE, 2-
CHLOROETHYL(ETHYL)SULPHIDE, 2-
2-CHLOROETHYL ETHYL SULFIDE [HSDB]
BETA-ETHYLMERKAPTOETHYLCHLORID (CZECH)
Halfmustard gas
2Ethylthioethyl chloride
Chlorothiolalcohol(CTA)
2(Ethylthio)chloroethane
Sulfide, diethyl 2chloro
1Chloro2(ethylthio)ethane
2Chloroethyl(ethyl)sulfide
Ethyl 2chloroethyl sulfide
betaEthylmerkaptoethylchlorid
Sulfide, 2chloroethyl ethyl
2Chloroethyl ethyl thioether
Ethyl betachloroethyl sulfide
Sulfide, diethyl, 2-chloro
Ethane, 1chloro2(ethylthio)
ETHYL (2-CHLOROETHYL) SULFIDE
211-742-1
gbnvxyxirhsyeg-uhfffaoysa-n
un1992
2-(Ethylthio)chloroethane
Ethyl 2-chloroethyl sulfide
2-Chloroethyl ethyl sulphide
Sulfide, 2-chloroethyl ethyl
1-chloro-2-ethylsulfanylethane
h-MG
Half-sulfur mustard
5MN267Q6RG
1-chloro-2-ethylsulfanyl-ethane
MFCD00000979
2-CEES
WLN: G2S2
SCHEMBL136233
CHEMBL3183525
ethyl (2-chloro-ethyl) sulfide
1-chloranyl-2-ethylsulfanyl-ethane
2-Chloroethyl ethyl sulfide, 97%
ALBB-008890
NSC10977
Tox21_200911
1-Chloro-2-(ethylsulfanyl)ethane #
STK505643
AKOS000321617
HY-W199190
NCGC00248873-01
NCGC00258465-01
AS-76116
CAS-693-07-2
FC118989
NS00036829
EN300-80329
D89330
A836424
Q26840793
Solubility of 1-chloro-2-ethylsulfanyl-ethane
1-chloro-2-ethylsulfanyl-ethane, with the chemical formula C4H9ClS, exhibits unique solubility characteristics that are important for its application in various fields.
Solubility Characteristics:
In summary, while 1-chloro-2-ethylsulfanyl-ethane presents challenges in terms of water solubility, it demonstrates compatibility with organic solvents, making it a versatile compound for various chemical processes.