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  2. Hydrazine - Wikipedia

    en.wikipedia.org/wiki/Hydrazine

    Hydrazine is an inorganic compound with the chemical formula N 2 H 4.It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour.Hydrazine is highly hazardous unless handled in solution as, for example, hydrazine hydrate (N 2 H 4 ·xH 2 O).

  3. 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can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou

  4. Category:Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Category:Hydrazines

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  5. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    When derived from hydrazine itself, hydrazones condense with a second equivalent of a carbonyl to give azines: [10] R 2 C=N−NH 2 + R 2 C=O → R 2 C=N−N=CR 2 + H 2 O. Hydrazones are intermediates in the Wolff–Kishner reduction. Hydrazones are reactants in hydrazone iodination, the Shapiro reaction, and the Bamford–Stevens reaction to ...

  6. Azane - Wikipedia

    en.wikipedia.org/wiki/Azane

    diazane (or hydrazine), N 2 H 4 - two nitrogen and four hydrogen triazane, N 3 H 5 - three nitrogen and five hydrogen. Azanes with three or more nitrogen atoms are named by adding the suffix-azane to the appropriate numerical multiplier prefix. Hence, triazane, N 3 H 5; tetrazane or tetraazane, N 4 H 6; pentazane or pentaazane, N 5 H 7 ...

  7. Hydrazide - Wikipedia

    en.wikipedia.org/wiki/Hydrazide

    An applied example is a synthesis of sunitinib begins by mixing 5-fluoroisatin slowly into hydrazine hydrate. [9] After 4 hours at 110 °C, the indole ring structure has been broken into (2-amino-5-fluoro-phenyl)-acetic acid hydrazide with reduction of the ketone at the 3-position.

  8. Wharton reaction - Wikipedia

    en.wikipedia.org/wiki/Wharton_reaction

    An α,β-epoxyketone reacts with hydrazine hydrate to yield an allylic alcohol. [ 7 ] In the synthesis of warburganal, a bioactive natural product, the α,β-epoxyketone is formed from a cyclic α,β-unsaturated ketone and in a separate step reacts under the classical Wharton olefin synthesis conditions to yield an allylic diol .

  9. Hydrazinium - Wikipedia

    en.wikipedia.org/wiki/Hydrazinium

    In the common names of such salts, the cation is often called "hydrazine", as in "hydrazine sulfate" for hydrazinium hydrogensulfate. The terms "hydrazinium" and "hydrazine" may also be used for the doubly protonated cation [N 2 H 6] 2+, more properly called hydrazinediium or hydrazinium(2+). This cation has an ethane-like structure ([H 3 N− ...