Interesting facts
Interesting Facts about 2-(diethylamino)ethanethiol
2-(diethylamino)ethanethiol, also known as DEAE-thiol, is a fascinating compound within the realm of organic chemistry. Its unique structure and properties make it of particular interest for various applications:
- Chemical Structure: The compound contains a thiol group (-SH), contributing to its reactivity and making it a strong nucleophile.
- Applications in Synthesis: Due to its thiol group, DEAE-thiol is often employed as a building block in the synthesis of other complex organic molecules. It plays a role in creating polymers and novel materials.
- Biological Importance: Thiols are known to be crucial in biological systems. For instance, they often participate in redox reactions, acting as antioxidants that protect against oxidative stress in living organisms.
- Electrophilic Addition Reactions: The presence of the amine and thiol groups in DEAE-thiol allows for interesting reactivity. It can participate in electrophilic addition reactions, making it valuable in the chemistry of amino acids and proteins.
- Potential Role in Drug Development: Due to its biological activities, 2-(diethylamino)ethanethiol may have potential applications in pharmacology, particularly in the development of new therapeutic agents.
Overall, 2-(diethylamino)ethanethiol is not just a simple compound; it embodies the intricate bond between structure and function in the chemistry of life. "The simplest compounds often lead to the most complex reactions." This illustrates the significance that such compounds hold in advancing both science and technology.
Synonyms
2-(Diethylamino)ethanethiol
100-38-9
Diethylcysteamine
Ethanethiol, 2-(diethylamino)-
Diethylcysteamin
Diethyl(2-mercaptoethyl)amine
Diethylaminoethanethiol
N-Diaethyl cysteamin
2-(Diethylamino)ethyl mercaptan
Triethylamine, 2-mercapto-
N-Diethyl cysteamine
N,N-Diethylcysteamine
N,N-Diethyl-cysteamine
NSC 49193
2-(Diethylamino)ethylmercaptan
N-Diaethyl cysteamin [German]
beta-Diethylaminoethyl mercaptan
EINECS 202-846-8
TF6S7Q84YD
BRN 0773677
2-(N,N-Diethylamino)ethanethiol
NSC-49193
(2-Mercaptoethyl)diethylamine
DTXSID1074414
4-04-00-01590 (Beilstein Handbook Reference)
N,N-(2-diethylamino)ethanethiol
DTXCID9032452
202-846-8
2-Diethylaminoethanethiol
2-(diethylamino)ethane-1-thiol
2-diethylamino-ethanethiol
2-(diethylamino)ethanthiol
N-diethylcysteamine
MFCD00066258
UNII-TF6S7Q84YD
2-(diethylamino)-ethanthiol
2-(diethylamino)-ethanethiol
2-Diethylaminoethyl mercaptan
diethyl(2-sulfanylethyl)amine
N,N-diethylaminoethylmercaptan
SCHEMBL295489
BDBM7970
WLN: SH2N2 & 2
.beta.-Diethylaminoethyl mercaptan
BCP11871
NSC49193
BBL011336
STL146426
AKOS005136505
NS00022976
A800190
F8881-2878
Solubility of 2-(diethylamino)ethanethiol
2-(diethylamino)ethanethiol, a compound characterized by its unique structure, showcases interesting solubility properties that are worthy of note. This compound is notable for being soluble in both polar and non-polar solvents, which makes it quite versatile in various chemical applications. Below are some key points regarding its solubility:
In conclusion, the solubility behavior of 2-(diethylamino)ethanethiol demonstrates its potential utility in diverse chemical processes. As one might say, *solubility is the key to reactivity and utility in chemistry.*