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  2. Methyl phenylacetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_phenylacetate

    Methyl phenylacetate is an organic compound that is the methyl ester of phenylacetic acid, with the structural formula C 6 H 5 CH 2 CO 2 CH 3. It is a colorless liquid that is only slightly soluble in water, but soluble in most organic solvents. Methyl phenylacetate has a strong odor similar to honey.

  3. Phenylacetic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylacetic_acid

    Phenylacetic acid (conjugate base phenylacetate), also known by various synonyms, is an organic compound containing a phenyl functional group and a carboxylic acid functional group. It is a white solid with a strong honey-like odor .

  4. 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).

  5. Methyl phenyldiazoacetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_phenyldiazoacetate

    Methyl phenyldiazoacetate is the organic compound with the formula C 6 H 5 C(N 2)CO 2 Me. It is a diazo derivative of methyl phenylacetate . Colloquially referred to as "phenyldiazoacetate", it is generated and used in situ after isolation as a yellow oil.

  6. Phenylacetone - Wikipedia

    en.wikipedia.org/wiki/Phenylacetone

    Phenylacetone, also known as phenyl-2-propanone, is an organic compound with the chemical formula C 6 H 5 CH 2 COCH 3.It is a colorless oil that is soluble in organic solvents.It is a mono-substituted benzene derivative, consisting of an acetone attached to a phenyl group.

  7. Phenyl acetate - Wikipedia

    en.wikipedia.org/wiki/Phenyl_acetate

    Phenyl acetate is the ester of phenol and acetic acid.It can be produced by reacting phenol with acetic anhydride or acetyl chloride.. Phenyl acetate can be separated into phenol and an acetate salt, via saponification: heating the phenyl acetate with a strong base, such as sodium hydroxide, will produce phenol and an acetate salt (sodium acetate, if sodium hydroxide were used).

  8. Category:Methyl esters - Wikipedia

    en.wikipedia.org/wiki/Category:Methyl_esters

    Pages in category "Methyl esters" The following 200 pages are in this category, out of approximately 303 total. ... Methyl perchlorate; Methyl phenylacetate; Methyl ...

  9. List of additives in cigarettes - Wikipedia

    en.wikipedia.org/wiki/List_of_additives_in...

    Methyl benzoate; Methyl cinnamate; Methyl dihydrojasmonate; Methyl ester of rosin, partially hydrogenated; Methyl isovalerate; Methyl linoleate (48%) Methyl linolenate (52%) mixture; Methyl naphthyl ketone; Methyl nicotinate; Methyl phenylacetate; Methyl salicylate; Methyl sulfide; 3-Methyl-1-cyclopentadecanone; 4-Methyl-1-phenyl-2-pentanone; 5 ...