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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.
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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 ...
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Sodium acetate trihydrate crystals melt at 58–58.4 °C (136.4–137.1 °F), [12] [13] dissolving in their water of crystallization [citation needed]. When they are heated past the melting point and subsequently allowed to cool, the aqueous solution becomes supersaturated .