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  2. Ethane-1,2-dithiol - Wikipedia

    en.wikipedia.org/wiki/Ethane-1,2-dithiol

    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.

  3. Ethane-1,1-dithiol - Wikipedia

    en.wikipedia.org/wiki/Ethane-1,1-dithiol

    In the presence of oxygen, ethane-1,1-dithiol is converted to cis/trans-3,6-dimethyl-1,2,4,5-tetrathiane which has a rubbery aroma. This molecule has a ring with four sulfur atoms and two carbons, two ethane-1,1-dithiol molecules become linked at their sulfur atoms with the loss of hydrogen. [ 11 ]

  4. Dithiol - Wikipedia

    en.wikipedia.org/wiki/Dithiol

    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.

  5. 1,2-ethanedithiol - Wikipedia

    en.wikipedia.org/?title=1,2-ethanedithiol&...

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  6. Ethanedithiol - Wikipedia

    en.wikipedia.org/wiki/Ethanedithiol

    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 ...

  7. List of CAS numbers by chemical compound - Wikipedia

    en.wikipedia.org/wiki/List_of_CAS_numbers_by...

    Chemical formula Synonyms CAS number C 10 H 16 N 2 O 8: Ethylenediaminetetraacetic acid (EDTA): 6381–92–6 C 12 H 22 O 11: sucrose: 57–50–1 C 18 H 29 O 3 S: sodium dodecyl benzenesulfonate: 2155–30–0

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  9. Thioacetal - Wikipedia

    en.wikipedia.org/wiki/Thioacetal

    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 ...