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  2. Phenyl salicylate - Wikipedia

    en.wikipedia.org/wiki/Phenyl_salicylate

    It is synthesized by heating salicylic acid with phenol in the presence of phosphoryl chloride. [4] It also arises from heating salicylic acid: [5] 2 HOC 6 H 4 CO 2 H → C 6 H 5 O 2 C 6 H 4 OH + CO 2 + H 2 O. The conversion entails dehydration and decarboxylation. Heating phenyl salicylate in turn gives xanthone. [6] [3]

  3. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    Phenol – the simplest of the phenols Chemical structure of salicylic acid, the active metabolite of aspirin Chemical structure of aloe emodin, a diphenol Quercetin, a typical flavonoid, is a polyphenol Tannic acid, a typical polyphenol of indeterminate structure Lignin, is around 25% of the composition of wood This structure is repeated many ...

  4. Phenolic acid - Wikipedia

    en.wikipedia.org/wiki/Phenolic_acid

    Chemical structure of salicylic acid, a common phenolic acid. Phenolic acids or phenolcarboxylic acids are phenolic compounds and types of aromatic acid compounds. Included in that class are substances containing a phenolic ring and an organic carboxylic acid function (C6-C1 skeleton).

  5. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of one or more hydroxyl groups (−O H) bonded directly to an aromatic hydrocarbon group. [1] The simplest is phenol, C 6 H 5 OH. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the ...

  6. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula C 6 H 5 OH. [5] It is a white crystalline solid that is volatile . The molecule consists of a phenyl group ( −C 6 H 5 ) bonded to a hydroxy group ( −OH ).

  7. The Ordinary Just Added to Its Cult-Fave Salicylic Acid Line ...

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  8. Sodium salicylate - Wikipedia

    en.wikipedia.org/wiki/Sodium_salicylate

    Sodium salicylate is a sodium salt of salicylic acid. It can be prepared from sodium phenolate and carbon dioxide under higher temperature and pressure. Historically, it has been synthesized by refluxing methyl salicylate (wintergreen oil) with an excess of sodium hydroxide. [4]

  9. 3-Methylsalicylic acid - Wikipedia

    en.wikipedia.org/wiki/3-Methylsalicylic_acid

    3-Methylsalicylic acid is an organic compound with the formula CH 3 C 6 H 3 (CO 2 H)(OH). It is a white solid that is soluble in basic water and in polar organic solvents. At neutral pH, the acid exists as 3-methylsalicylate Its functional groups include a carboxylic acid and a phenol group. It is one of four isomers of methylsalicylic acid.

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