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  2. 4-Aminophenol - Wikipedia

    en.wikipedia.org/wiki/4-Aminophenol

    4-Aminophenol (or para-aminophenol or p-aminophenol) is an organic compound with the formula H 2 NC 6 H 4 OH. Typically available as a white powder, [ 3 ] it is commonly used as a developer for black-and-white film , marketed under the name Rodinal .

  3. Aminophenol - Wikipedia

    en.wikipedia.org/wiki/Aminophenol

    The three aminophenol isomers: Left: 2-Aminophenol (o-aminophenol) Center: 3-Aminophenol (m-aminophenol) Right: 4-Aminophenol (p-aminophenol) Aminophenol may refer to any of three isomeric chemical compounds: 2-Aminophenol; 3-Aminophenol; 4-Aminophenol; They are simultaneously an aniline and a phenol

  4. Category:4-Aminophenyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:4-Aminophenyl...

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  5. Category:Aminophenols - Wikipedia

    en.wikipedia.org/wiki/Category:Aminophenols

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  6. 2-Aminophenol - Wikipedia

    en.wikipedia.org/wiki/2-Aminophenol

    2-Aminophenol is an organic compound with the formula C 6 H 7 NO. Along with its isomer 4-aminophenol , it is an amphoteric molecule and a reducing agent . It is a useful reagent for the synthesis of dyes and heterocyclic compounds . [ 3 ]

  7. C6H7NO - Wikipedia

    en.wikipedia.org/wiki/C6H7NO

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... 3-Aminophenol; 4-Aminophenol; Nicotinyl alcohol;

  8. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    However, this synthesis risks the self-condensation of alcohol itself (e.g. ethanol self-condenses to form diethyl ether). A more common and higher-yielding reaction is the Williamson ether synthesis , where a phenol is converted by a strong base to the phenoxide ion, which can subsequently be reacted with an alkyl halide via nucleophilic ...

  9. File:4-Aminophenol.svg - Wikipedia

    en.wikipedia.org/wiki/File:4-Aminophenol.svg

    Original file (SVG file, nominally 369 × 821 pixels, file size: 4 KB) This is a file from the Wikimedia Commons . Information from its description page there is shown below.

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