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  2. 1-Naphthol - Wikipedia

    en.wikipedia.org/wiki/1-naphthol

    1-Naphthol, or α-naphthol, is a organic compound with the formula C 10 H 7 OH. It is a fluorescent white solid. 1-Naphthol differs from its isomer 2-naphthol by the location of the hydroxyl group on the naphthalene ring.

  3. Category:1-Naphthols - Wikipedia

    en.wikipedia.org/wiki/Category:1-Naphthols

    This page was last edited on 14 November 2024, at 15:02 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  4. Naphthol - Wikipedia

    en.wikipedia.org/wiki/Naphthol

    Naphthol may refer to: 1-Naphthol; 2-Naphthol This page was last edited on 26 June 2023, at 00:21 (UTC). Text is available under the Creative Commons Attribution ...

  5. Naphthalene - Wikipedia

    en.wikipedia.org/wiki/Naphthalene

    Naphthalenesulfonic acids are used in the synthesis of 1-naphthol and 2-naphthol, precursors for various dyestuffs, pigments, rubber processing chemicals and other chemicals and pharmaceuticals. [25] They are also used as dispersants in synthetic and natural rubbers, in agricultural pesticides, in dyes, and in lead–acid battery plates.

  6. 2-Naphthol - Wikipedia

    en.wikipedia.org/wiki/2-Naphthol

    2-Naphthol, or β-naphthol, is a fluorescent colorless (or occasionally yellow) crystalline solid with the formula C 10 H 7 OH. It is an isomer of 1-naphthol, differing by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol, but more reactive.

  7. List of dyes - Wikipedia

    en.wikipedia.org/wiki/List_of_dyes

    β-naphthol Azoic coupling component 1 37500 diazonium salt 135-19-3: Naphthol green B: Acid green 1 10020 nitroso 19381-50-1: Naphthol yellow S: Sulfur yellow S Acid yellow 1 Food yellow 1 10316 nitro 846-70-8: Naphthylamin Brown F Acid brown 6 14625 azo 6419-10-5: Neutral red: Toluylene red Basic red 5 50040 eurhodin 553-24-2: New fuchsine ...

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  9. Bucherer reaction - Wikipedia

    en.wikipedia.org/wiki/Bucherer_reaction

    The reaction is used to convert 1,7-dihydroxynaphthalene into 7-amino-1-naphthol and 1-aminonaphthalene-4-sulfonic acid into 1-hydroxynaphthalene-4-sulfonic acid. It is also useful for transamination reactions of 2-aminonaphthalenes .

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