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  2. Thiol - Wikipedia

    en.wikipedia.org/wiki/Thiol

    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.

  3. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    Some sulfides are named by modifying the common name for the corresponding ether. For example, C 6 H 5 SCH 3 is methyl phenyl sulfide, but is more commonly called thioanisole, since its structure is related to that for anisole, C 6 H 5 OCH 3. The modern systematic nomenclature in chemistry for the trival name thioether is sulfane. [2]

  4. Category:Thiols - Wikipedia

    en.wikipedia.org/wiki/Category:Thiols

    Download QR code; Print/export Download as PDF; Printable version; ... Pages in category "Thiols" The following 91 pages are in this category, out of 91 total.

  5. Thiophenol - Wikipedia

    en.wikipedia.org/wiki/Thiophenol

    Thiophenol is an organosulfur compound with the formula C 6 H 5 SH, sometimes abbreviated as PhSH. This foul-smelling colorless liquid is the simplest aromatic thiol.The chemical structures of thiophenol and its derivatives are analogous to phenols, where the oxygen atom in the hydroxyl group (-OH) bonded to the aromatic ring in phenol is replaced by a sulfur atom.

  6. Sulfide - Wikipedia

    en.wikipedia.org/wiki/Sulfide

    Some metal sulfides, when exposed to a strong mineral acid, including gastric acids, will release toxic hydrogen sulfide. Organic sulfides are highly flammable. When a sulfide burns it produces sulfur dioxide (SO 2) gas. Hydrogen sulfide, some of its salts, and almost all organic sulfides have a strong and putrid stench; rotting biomass ...

  7. Category:Sulfides - Wikipedia

    en.wikipedia.org/wiki/Category:Sulfides

    Download QR code; Print/export Download as PDF; Printable version; ... Pages in category "Sulfides" The following 81 pages are in this category, out of 81 total.

  8. Propanethiol - Wikipedia

    en.wikipedia.org/wiki/Propanethiol

    Propanethiol is an organic compound with the molecular formula C 3 H 8 S. It belongs to the group of thiols.It is a colorless liquid with a strong, offensive odor. It is moderately toxic and is less dense than water and slightly soluble in water.

  9. Thioester - Wikipedia

    en.wikipedia.org/wiki/Thioester

    Thioesters can be prepared by condensation of thiols and carboxylic acids in the presence of dehydrating agents: [2] [3] RSH + R'CO 2 H → RSC(O)R' + H 2 O. A typical dehydration agent is DCC. [4] Efforts to improve the sustainability of thioester synthesis have also been reported utilising safer coupling reagent T3P and greener solvent ...