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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. C6H7NO - Wikipedia

    en.wikipedia.org/wiki/C6H7NO

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; ... 2-Aminophenol; 3-Aminophenol; 4-Aminophenol; Nicotinyl alcohol;

  4. 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

  5. 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 ]

  6. Category:Aminophenols - Wikipedia

    en.wikipedia.org/wiki/Category:Aminophenols

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikimedia Commons; ... Aminophenol; 2-Aminophenol; 3-Aminophenol; 4-Aminophenol; G.

  7. Bamberger rearrangement - Wikipedia

    en.wikipedia.org/wiki/Bamberger_rearrangement

    The mechanism of the Bamberger rearrangement proceeds from the monoprotonation of N-phenylhydroxylamine 1.N-protonation 2 is favored, but unproductive. O-protonation 3 can form the nitrenium ion 4, which can react with nucleophiles (H 2 O) to form the desired 4-aminophenol 5.

  8. 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.

  9. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    Amyl alcohol isomers; Common name Structure Type IUPAC name Boiling point (°C) [3] 1-pentanol or normal amyl alcohol primary Pentan-1-ol: 138.5 2-methyl-1-butanol or active amyl alcohol primary 2-Methylbutan-1-ol: 128.7 3-methyl-1-butanol or isoamyl alcohol or isopentyl alcohol primary 3-Methylbutan-1-ol: 131.2 2,2-dimethyl-1-propanol or ...

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