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  2. Methyl benzoate - Wikipedia

    en.wikipedia.org/wiki/Methyl_benzoate

    Density: 1.0837 g/cm 3: ... data are given for materials in their standard state (at 25 °C [77 °F], ... Methyl benzoate is an organic compound.

  3. 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 ...

  4. Methyl 4-iodobenzoate - Wikipedia

    en.wikipedia.org/wiki/Methyl_4-iodobenzoate

    Methyl 4-iodobenzoate, or methyl p-iodobenzoate, is an organic compound with the formula IC 6 H 4 COOCH 3. [3] It is the methyl ester of 4-iodobenzoic acid , or may also be viewed as an iodinated derivative of methyl benzoate .

  5. Triphenylmethanol - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethanol

    Density: 1.199 g/cm 3: ... data are given for ... The preparation of triphenylmethanol from methyl benzoate or benzophenone and phenylmagnesium bromide is a common ...

  6. Propyl benzoate - Wikipedia

    en.wikipedia.org/wiki/Propyl_benzoate

    Density: 1.0230 g/cm 3 at 20 ... data are given for materials in their standard state ... Propyl benzoate can be synthesized by the transesterification of methyl ...

  7. Methyl anthranilate - Wikipedia

    en.wikipedia.org/wiki/Methyl_anthranilate

    Methyl anthranilate, also known as MA, methyl 2-aminobenzoate, or carbomethoxyaniline, is an ester of anthranilic acid. Its chemical formula is C 8 H 9 NO 2 . It has a strong and fruity grape smell, and one of its key uses is as a flavoring agent.

  8. 3-Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3-Nitrobenzoic_acid

    3-Nitrobenzoic acid is an organic compound with the formula C 6 H 4 (NO 2)CO 2 H. It is an aromatic compound and under standard conditions, it is an off-white solid. The two substituents are in a meta position with respect to each other, giving the alternative name of m-nitrobenzoic acid.

  9. 3,5-Dinitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3,5-Dinitrobenzoic_acid

    3,5-Dinitrobenzoic acid finds use in the identification of various organic substances, especially alcohols, by derivatization.For such an analysis, the substance to be analyzed is reacted with 3,5-dinitrobenzoic acid in the presence of sulfuric acid in order to form a derivate.