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  2. Furaneol - Wikipedia

    en.wikipedia.org/wiki/Furaneol

    Furaneol, or strawberry furanone, is an organic compound used in the flavor and perfume industry. ... The acetate ester of furaneol, ...

  3. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).

  4. Furfuryl alcohol - Wikipedia

    en.wikipedia.org/wiki/Furfuryl_alcohol

    Furfuryl alcohol is manufactured industrially by hydrogenation of furfural, which is itself typically produced from waste bio-mass such as corncobs or sugar cane bagasse.As such furfuryl alcohol may be considered a green chemical. [5]

  5. Ester - Wikipedia

    en.wikipedia.org/wiki/Ester

    An ester of a carboxylic acid.R stands for any group (typically hydrogen or organyl) and R ′ stands for any organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (R ′). [1]

  6. Aroma compound - Wikipedia

    en.wikipedia.org/wiki/Aroma_compound

    Fragrance bottles. An aroma compound, also known as an odorant, aroma, fragrance or flavoring, is a chemical compound that has a smell or odor.For an individual chemical or class of chemical compounds to impart a smell or fragrance, it must be sufficiently volatile for transmission via the air to the olfactory system in the upper part of the nose.

  7. 2-Furanone - Wikipedia

    en.wikipedia.org/wiki/2-furanone

    2-Furanone is prepared by oxidation of furfural: [2]. It exists in equilibrium with the tautomer 2-hydroxyfuran, which serves as an intermediate in the interconversion between the β- and α-furanones.

  8. Fischer–Speier esterification - Wikipedia

    en.wikipedia.org/wiki/Fischer–Speier...

    As a result, ethyl acetate—the ester of ethanol and acetic acid—is the most abundant ester in wines. Other combinations of organic alcohols (such as phenol-containing compounds) and organic acids lead to a variety of different esters in wines, contributing to their different flavours, smells and tastes.

  9. -oate - Wikipedia

    en.wikipedia.org/wiki/-oate

    The suffix-oate is the IUPAC nomenclature used in organic chemistry to form names of compounds formed with ester. They are of two types: They are of two types: Formed by replacing the hydrogen atom in the –COOH by some other radical , usually an alkyl or aryl radical forming an ester .