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  2. 4-Hydroxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-hydroxybenzaldehyde

    4Hydroxy­benzaldehyde (para‑hydroxy­benzaldehyde) is an organic compound with the formula C 6 H 4 OH(CHO). [4] [5] Along with 2-hydroxybenzaldehyde and 3-hydroxybenzaldehyde, it is one of the three isomers of hydroxybenzaldehyde.

  3. 2-Hydroxy-4-methoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-Hydroxy-4...

    2-Hydroxy-4-methoxybenzaldehyde is a chemical compound and an isomer of vanillin. Urolithin M7 , one of the urolithins , has also been synthesized from 2-hydroxy-4-methoxybenzaldehyde using the inverse electron-demand Diels–Alder reaction .

  4. Salicylaldehyde - Wikipedia

    en.wikipedia.org/wiki/Salicylaldehyde

    Salicylaldehyde is produced by condensation of phenol with formaldehyde to give hydroxybenzyl alcohol, which is oxidized to the aldehyde. [4] Salicylaldehydes in general are prepared by ortho-selective formylation reactions from the corresponding phenol, for instance by the Duff reaction, Reimer–Tiemann reaction, or by treatment with paraformaldehyde in the presence of magnesium chloride and ...

  5. Vanillin - Wikipedia

    en.wikipedia.org/wiki/Vanillin

    Vanillin is an organic compound with the molecular formula C 8 H 8 O 3.It is a phenolic aldehyde.Its functional groups include aldehyde, hydroxyl, and ether.It is the primary component of the extract of the vanilla bean.

  6. Vanillic acid - Wikipedia

    en.wikipedia.org/wiki/Vanillic_acid

    Vanillic acid (4-hydroxy-3-methoxybenzoic acid) is a dihydroxybenzoic acid derivative used as a flavoring agent. It is an oxidized form of vanillin. It is also an intermediate in the production of vanillin from ferulic acid. [2] [3]

  7. 2-Hydroxy-5-methoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-Hydroxy-5...

    The chemical is produced by the Reimer-Tiemann reaction on 4-methoxyphenol with a 79% yield. [1] It reacts with malononitrile to form 2-imino-6-methoxy-2H-1-benzopyran-3-carbonitrile. [2] It can be reduced by sodium borohydride in ethanol to form 2-hydroxy-5-methoxybenzyl alcohol. [3]

  8. ortho-Vanillin - Wikipedia

    en.wikipedia.org/wiki/Ortho-vanillin

    ortho-Vanillin (2-hydroxy-3-methoxybenzaldehyde) is an organic solid present in the extracts and essential oils of many plants. [1] [2] [3] Its functional groups include aldehyde, ether and phenol. ortho-Vanillin, a compound of the formula C 8 H 8 O 3, is distinctly different from its more prevalent isomer, meta-vanillin.

  9. 5-Nitrovanillin - Wikipedia

    en.wikipedia.org/wiki/5-nitrovanillin

    5-Nitrovanillin (4-hydroxy-3-methoxy-5-nitrobenzaldehyde) is a derivative of vanillin in which the hydrogen ortho- to the hydroxy group is substituted by a nitro group.