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  2. Methyl benzoate - Wikipedia

    en.wikipedia.org/wiki/Methyl_benzoate

    Methyl benzoate is an organic compound. It is an ester with the chemical formula C 6 H 5 COOCH 3 , sometimes abbreviated as PhCO 2 Me , where Ph and Me are phenyl and methyl , respectively. Its structure is C 6 H 5 −C(=O)−O−CH 3 .

  3. File:Methyl benzoate.svg - Wikipedia

    en.wikipedia.org/wiki/File:Methyl_benzoate.svg

    The following other wikis use this file: Usage on azb.wikipedia.org متل بنزوات; Usage on bs.wikipedia.org Ester; Usage on el.wikipedia.org

  4. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Benzyl group and derivatives: Benzyl group, benzyl radical, benzyl amine, benzyl bromide, benzyl chloroformate, and benzyl methyl ether. R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5.

  5. -oate - Wikipedia

    en.wikipedia.org/wiki/-oate

    For example, methyl benzoate is a molecular compound with the structure C 6 H 5 –CO–O–CH 3, and its condensed structural formula usually written as C 6 H 5 COOCH 3. Formed by removing the hydrogen atom in the –COOH, producing an anion, which joins with a cation forming a salt.

  6. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    In organic chemistry, benzoyl (/ ˈ b ɛ n z oʊ ɪ l /, BENZ-oh-il) [1] is the functional group with the formula −COC 6 H 5 and structure −C(=O)−C 6 H 5. [2] [3] It can be viewed as benzaldehyde missing one hydrogen. The benzoyl group has a mass of 105 amu. The term "benzoyl" should not be confused with benzyl, which has the formula − ...

  7. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    The efficacy of benzoic acid and benzoate is thus dependent on the pH of the food. [24] Benzoic acid, benzoates and their derivatives are used as preservatives for acidic foods and beverages such as citrus fruit juices ( citric acid ), sparkling drinks ( carbon dioxide ), soft drinks ( phosphoric acid ), pickles ( vinegar ) and other acidified ...

  8. Paraben - Wikipedia

    en.wikipedia.org/wiki/Paraben

    The Arrhenius equation was used in a study to calculate activation energies for the chlorination of four parent parabens (methyl-, ethyl-, propyl-, and butylparaben) and was found to range from 36–47 kJ/mol. [21] In another study, tap water at 20 °C (68 °F) containing 50–200 μM free chlorine was spiked with 0.5 μM propylparaben and the ...

  9. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/Phenyl_group

    Phenyl radical group. In organic chemistry, the phenyl group, or phenyl ring, is a cyclic group of atoms with the formula C6H5, and is often represented by the symbol Ph (archaically φ) or Ø.