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Ethane-1,2-dithiol, also known as EDT, [1] is a colorless liquid with the formula C 2 H 4 2. It has a very characteristic odor which is compared by many people to rotten cabbage . It is a common building block in organic synthesis and an excellent ligand for metal ions.
The salt can be generated quantitatively by reaction with sodium hydride. [14] Ethanethiol can be oxidized to ethyl sulfonic acid, using strong oxidizing agents. Weaker oxidants, such as ferric oxide or hydrogen peroxide give the disulfide, diethyl disulfide: 2 EtSH + H 2 O 2 → EtS-SEt + 2 H 2 O. Like other thiols, it behaves comparably to ...
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Dithioacetals generated from aldehydes and either 1,2-ethanedithiol or 1,3-propanedithiol are especially common among this class of molecules for use in organic synthesis. [ 2 ] The carbonyl carbon of an aldehyde is electrophilic and therefore susceptible to attack by nucleophiles , whereas the analogous central carbon of a dithioacetal is not ...
Ethanedithiol may refer to: 1,1-Ethanedithiol; 1,2-Ethanedithiol; See also. Methanedithiol This page was last edited on 18 July 2024, at 03:17 (UTC). Text is ...
Geminal dithiols have the formula RR'C(SH) 2. They are derived from aldehydes and ketones by the action of hydrogen sulfide. Their stability contrasts with the rarity of geminal diols. Examples include methanedithiol, ethane-1,1-dithiol, and cyclohexane-1,1-dithiol.
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Thiol with a blue highlighted sulfhydryl group.. In organic chemistry, a thiol (/ ˈ θ aɪ ɒ l /; [1] from Ancient Greek θεῖον (theion) 'sulfur' [2]), or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent.
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