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In organic chemistry, "sulfide" usually refers to the linkage C–S–C, although the term thioether is less ambiguous. For example, the thioether dimethyl sulfide is CH 3 –S–CH 3. Polyphenylene sulfide (see below) has the empirical formula C 6 H 4 S. Occasionally, the term sulfide refers to molecules containing the –SH functional group.
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]
Methyl Sulfide. Add languages. Add links. ... Print/export Download as PDF ... In other projects Appearance. move to sidebar hide. From Wikipedia, the free ...
β-Naphthol methyl ether: 93-04-9 C 11 H 11 NO 2: 3-indolepropionic acid: 830-96-6 C 11 H 12 N 2 O 2: tryptophan Trp: 73-22-3 C 11 H 12 O 3: myristicin: C 11 H 13 NO 6: Caramboxin or Diroximel fumarate: C 11 H 14 N 2 O: 5-methoxytryptamine: 608-07-1 C 11 H 14 O 2: methyl eugenol: C 11 H 14 O 2: methyl isoeugenol: C 11 H 16 O 2: Jasmolone: 54383 ...
Also acid ionization constant or acidity constant. A quantitative measure of the strength of an acid in solution expressed as an equilibrium constant for a chemical dissociation reaction in the context of acid-base reactions. It is often given as its base-10 cologarithm, p K a. acid–base extraction A chemical reaction in which chemical species are separated from other acids and bases. acid ...
The compound (C 5 H 5) 2 TiS 5 is an example of a polysulfide complex. Polysulfides are a class of chemical compounds derived from anionic chains of sulfur atoms. [1] There are two main classes of polysulfides: inorganic and organic. The inorganic polysulfides have the general formula S 2− n. These anions are the conjugate bases of ...
German chemist Hermann Kolbe discovered MSA between 1842 and 1845 and originally termed it methyl hyposulphuric acid. [ 4 ] [ 5 ] [ 6 ] The discovery stemmed from earlier work by Berzelius and Marcet in 1813, who treated carbon disulfide with moist chlorine and produced a compound they named "sulphite of chloride of carbon".
A common example is sodium lauryl sulfate, with the formula CH 3 (CH 2) 11 OSO 3 Na. Also common in consumer products are the sulfate esters of ethoxylated fatty alcohols such as those derived from lauryl alcohol. An example is sodium laureth sulfate, an ingredient in some cosmetics. [2]