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  2. Benzophenone imine - Wikipedia

    en.wikipedia.org/wiki/Benzophenone_imine

    Benzophenone imine is an organic compound with the formula of (C 6 H 5) 2 C=NH. A pale yellow liquid, benzophenone imine is used as a reagent in organic synthesis. [1]

  3. Benzophenone - Wikipedia

    en.wikipedia.org/wiki/Benzophenone

    Benzophenone is a naturally occurring organic compound with the formula (C 6 H 5) 2 CO, generally abbreviated Ph 2 CO. Benzophenone has been found in some fungi, fruits and plants, including grapes. [4] It is a white solid with a low melting point and rose-like odor [5] that is soluble in organic solvents. Benzophenone is the simplest ...

  4. C13H11N - Wikipedia

    en.wikipedia.org/wiki/C13H11N

    Benzophenone imine, an organic compound with the formula of (C 6 H 5) 2 C=NH; 2-Aminofluorene, a synthetic arylamine This page was last edited on 28 February 2023, at ...

  5. Imine - Wikipedia

    en.wikipedia.org/wiki/Imine

    When R = H, the compound is a primary imine, when R is hydrocarbyl, the compound is a secondary imine. If this group is not a hydrogen atom, then the compound can sometimes be referred to as a Schiff base. [9] When R 3 is OH, the imine is called an oxime, and when R 3 is NH 2 the imine is called a hydrazone.

  6. Stetter reaction - Wikipedia

    en.wikipedia.org/wiki/Stetter_reaction

    The Stetter reaction is a reaction used in organic chemistry to form carbon-carbon bonds through a 1,4-addition reaction utilizing a nucleophilic catalyst. [1] While the related 1,2-addition reaction, the benzoin condensation, was known since the 1830s, the Stetter reaction was not reported until 1973 by Dr. Hermann Stetter. [2]

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  9. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    Benzophenone hydrazone, an illustrative hydrazone ... Imine; Nitrosamine; ... This page was last edited on 20 October 2024, at 13:23 (UTC).

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