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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.
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 ...
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.
In the diluted form with 4% ethyl acetate and ethanol the CAS number is 69382-62-3. [3] Toxicity may be due to metabolism products hydrogen sulfide and acetaldehyde , however as used it has a margin of safety of over 10,000,000. [ 2 ]
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 ...
1,3-Dithiolane is the organosulfur compound with the formula CH 2 S 2 C 2 H 4. Also classified as a heterocycle related cyclopentane by replacing two methylene bridges (-CH 2 - units) with thioether groups. It is an isomer of 1,2-dithiolane. [1] 1,3-Dithiolanes are compounds where one or more H atoms of the parent 1,3-dithiolane are replaced by ...
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Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH 3 CH 2 SH. [5] It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of ...