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  2. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    General structure of a sulfide with the blue marked functional group. In organic chemistry, a sulfide (British English sulphide) or thioether is an organosulfur functional group with the connectivity R−S−R' as shown on right. Like many other sulfur-containing compounds, volatile sulfides have foul odors. [1]

  3. Sulfide - Wikipedia

    en.wikipedia.org/wiki/Sulfide

    Sulfide (also sulphide in British English) [2] is an inorganic anion of sulfur with the chemical formula S 2− or a compound containing one or more S 2− ions. Solutions of sulfide salts are corrosive. Sulfide also refers to large families of inorganic and organic compounds, e.g. lead sulfide and dimethyl sulfide.

  4. Glossary of chemical formulae - Wikipedia

    en.wikipedia.org/wiki/Glossary_of_chemical_formulae

    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 ...

  5. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    [15] [16] The term "methyl" was derived in about 1840 by back-formation from "methylene", and was then applied to describe "methyl alcohol" (which since 1892 is called "methanol"). Methyl is the IUPAC nomenclature of organic chemistry term for an alkane (or alkyl) molecule, using the prefix "meth-" to indicate the presence of a single carbon.

  6. Dimethyl sulfide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfide

    Dimethyl sulfide has a characteristic odor commonly described as cabbage-like.It becomes highly disagreeable at even quite low concentrations. Some reports claim that DMS has a low olfactory threshold that varies from 0.02 to 0.1 ppm [clarification needed] between different persons, but it has been suggested that the odor attributed to dimethyl sulfide may in fact be due to disulfides ...

  7. Allyl methyl sulfide - Wikipedia

    en.wikipedia.org/wiki/Allyl_methyl_sulfide

    Allyl methyl sulfide is an organosulfur compound with the chemical formula CH 2 =CHCH 2 SCH 3. The molecule features two functional groups, an allyl (CH 2 =CHCH 2) and a sulfide. It is a colourless liquid with a strong odor characteristic of alkyl sulfides. It is a metabolite of garlic, and "garlic breath" is attributed to its presence. [1]

  8. Polysulfide - Wikipedia

    en.wikipedia.org/wiki/Polysulfide

    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 ...

  9. Sulfonyl group - Wikipedia

    en.wikipedia.org/wiki/Sulfonyl_group

    Sulfonyl groups can be reduced to the sulfide with diisobutylaluminium hydride (DIBALH). Lithium aluminium hydride (LiAlH 4) reduces some but not all sulfones to sulfides. [1]: 1851 In inorganic chemistry, when the group −S(=O) 2 − is not connected to any carbon atoms, it is referred to as sulfuryl. [3]