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  2. 3,4-Ethylenedioxythiophene - Wikipedia

    en.wikipedia.org/wiki/3,4-ethylenedioxythiophene

    3,4-Ethylenedioxythiophene (EDOT) is an organosulfur compound with the formula C 2 H 4 O 2 C 4 H 2 S. The molecule consists of thiophene, substituted at the 3 and 4 positions with an ethylene glycolyl unit.

  3. Thiophene - Wikipedia

    en.wikipedia.org/wiki/Thiophene

    Thiophene is considered to be aromatic, although theoretical calculations suggest that the degree of aromaticity is less than that of benzene. The "electron pairs" on sulfur are significantly delocalized in the pi electron system. As a consequence of its aromaticity, thiophene does not exhibit the properties seen for conventional sulfides. For ...

  4. Category:Thiophenes - Wikipedia

    en.wikipedia.org/wiki/Category:Thiophenes

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  5. Thienothiophene - Wikipedia

    en.wikipedia.org/wiki/Thienothiophene

    Thieno[3,2-b]thiophene. In organic chemistry, thienothiophene is any of several compounds consisting of two fused thiophene rings. They have the molecular formula C 6 H 4 S 2. Three constitutional isomers have been synthesized: thieno[3,2-b]thiophene, thieno[2,3-b]thiophene, and thieno[3,4-b]thiophene. The other isomer features S(IV) and is ...

  6. Thiofentanyl - Wikipedia

    en.wikipedia.org/wiki/Thiofentanyl

    Thiofentanyl is an opioid analgesic that is an analogue of fentanyl.. Thiofentanyl was sold briefly on the black market in the early 1980s, before the introduction of the Federal Analog Act which for the first time attempted to control entire families of drugs based on their structural similarity rather than scheduling each drug individually as they appeared. [1]

  7. Polythiophene - Wikipedia

    en.wikipedia.org/wiki/Polythiophene

    A carbocation mechanism is inferred from the structure of 3-(4-octylphenyl)thiophene prepared from ferric chloride. [33] Polymerization of thiophene can be effected by a solution of ferric chloride in acetonitrile. The kinetics of thiophene polymerization also seemed to contradict the predictions of the radical polymerization mechanism. [63]

  8. Thiophene-2-acetic acid - Wikipedia

    en.wikipedia.org/wiki/Thiophene-2-acetic_acid

    Thiophene-2-acetic acid is the organosulfur compound with the formula HO 2 CCH 2 C 4 H 3 S. Together with thiophene-3-acetic acid, it is one of two isomeric thiophene acetic acids. Preparation and use

  9. Tetrahydrothiophene - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrothiophene

    Both unsubstituted and substituted tetrahydrothiophenes are reported to occur in nature. For example, tetrahydrothiophene occurs as a volatile from Eruca sativa Mill. . (salad rocket) [5] while monocyclic substituted tetrahydrothiophenes have been isolated from Allium fistulosum 'Kujou', [6] Allium sativum (garlic), [7] Allium cepa (onion), [8] Allium schoenoprasum (chives), [9] and Salacia ...