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  2. Selenium compounds - Wikipedia

    en.wikipedia.org/wiki/Selenium_compounds

    Selenium disulfide has been used in shampoo as an antidandruff agent, an inhibitor in polymer chemistry, a glass dye, and a reducing agent in fireworks. [6] Selenium trioxide may be synthesized by dehydrating selenic acid, H 2 SeO 4, which is itself produced by the oxidation of selenium dioxide with hydrogen peroxide: [8]

  3. Selenium disulfide - Wikipedia

    en.wikipedia.org/wiki/Selenium_disulfide

    Selenium disulfide, also known as selenium sulfide, is a chemical compound and medication used to treat seborrheic dermatitis, dandruff, and pityriasis versicolor. [ 1 ] [ 2 ] It is applied to the affected area as a lotion or shampoo. [ 3 ]

  4. Selenium - Wikipedia

    en.wikipedia.org/wiki/Selenium

    Selenium is a chemical element; it has the symbol Se and atomic number 34. It has various physical appearances, including a brick-red powder, a vitreous black solid, and a grey metallic-looking form. It seldom occurs in this elemental state or as pure ore compounds in Earth's crust.

  5. Sulfoxide - Wikipedia

    en.wikipedia.org/wiki/Sulfoxide

    In organic chemistry, a sulfoxide, also called a sulphoxide, is an organosulfur compound containing a sulfinyl (>SO) functional group attached to two carbon atoms. It is a polar functional group. Sulfoxides are oxidized derivatives of sulfides .

  6. Selenium sulfide - Wikipedia

    en.wikipedia.org/wiki/Selenium_sulfide

    Selenium hexasulfide, Se 2 S 6 Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.

  7. Selenosulfide - Wikipedia

    en.wikipedia.org/wiki/Selenosulfide

    Simplest is the material selenium sulfide, which has medicinal properties. It adopt the diverse structures of elemental sulfur but with some S atoms replaced by Se. Other inorganic selenide sulfide compounds occur as minerals and as pigments. One example is antimony selenosulfide.

  8. Selenoxide elimination - Wikipedia

    en.wikipedia.org/wiki/Selenoxide_elimination

    Analogous sulfoxide eliminations are generally harder to implement than selenoxide eliminations. Formation of the carbon–sulfur bond is usually accomplished with highly reactive sulfenyl chlorides, which must be prepared for immediate use. However, sulfoxides are more stable than the corresponding selenoxides, and elimination is usually ...

  9. Sulfur compounds - Wikipedia

    en.wikipedia.org/wiki/Sulfur_compounds

    The simplest sulfoxide, dimethyl sulfoxide, is a common solvent; a common sulfone is sulfolane. Sulfonic acids are used in many detergents. Compounds with carbon–sulfur multiple bonds are uncommon, an exception being carbon disulfide, a volatile colorless liquid that is structurally similar to carbon dioxide.