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  2. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. . Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou

  3. Phenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/Phenylhydrazine

    Phenylhydrazine was the first hydrazine derivative characterized, reported by Hermann Emil Fischer in 1875. [7] [8] He prepared it by reduction of a phenyl diazonium salt using sulfite salts. Fischer used phenylhydrazine to characterize sugars via formation of hydrazones known as osazones with the sugar aldehyde. He also demonstrated in this ...

  4. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  5. 2,4-Dinitrophenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenylhydrazine

    Print/export Download as PDF; ... Safety data sheet (SDS) MSDS: ... data are given for materials in their standard state (at 25 °C ...

  6. 2-Phenylethyl bromide - Wikipedia

    en.wikipedia.org/wiki/2-Phenylethyl_bromide

    2-Phenylethyl bromide is an organobromide with the formula C 6 H 5 CH 2 CH 2 Br. It is a colorless liquid, although older samples appear yellow. Analogous to the preparation of most 1-bromoalkanes, it is prepared by free-radical addition of hydrogen bromide to styrene.

  7. p-Toluenesulfonyl hydrazide - Wikipedia

    en.wikipedia.org/wiki/P-toluenesulfonyl_hydrazide

    The compound is an important reagent in organic synthesis, serving as a source of reactive diimide and its subsequent chemical reactions. It condenses with ketones and aldehydes to form hydrazones, which can be further transformed into reactive intermediates such as diazo compounds or carbenes.

  8. Phenylethylidenehydrazine - Wikipedia

    en.wikipedia.org/wiki/Phenylethylidenehydrazine

    Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... Chemical and physical data; Formula: C 8 H 10 N 2: Molar mass: 134.182 g·mol − ...

  9. Fischer indole synthesis - Wikipedia

    en.wikipedia.org/wiki/Fischer_indole_synthesis

    The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a (substituted) phenylhydrazine and an aldehyde or ketone under acidic conditions. [1] [2] The reaction was discovered in 1883 by Emil Fischer. Today antimigraine drugs of the triptan class are often synthesized by this method. The Fischer ...