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  2. Phenethyl acetate - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_acetate

    Phenethyl acetate is the ester resulting from the condensation of acetic acid and phenethyl alcohol. Like many esters, it is found in a range of fruits and biological products. [ 1 ] It is a colorless liquid with a rose and honey scent and a raspberry-like taste.

  3. 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).

  4. Phenethyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_alcohol

    Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH. It is a colourless liquid with a pleasant floral odor. It is a colourless liquid with a pleasant floral odor.

  5. Precursor chemicals - Wikipedia

    en.wikipedia.org/wiki/Precursor_chemicals

    Drug precursors, also referred to as precursor chemicals or simply precursors, are substances used to manufacture illicit drugs.Most precursors also have legitimate commercial uses and are legally used in a wide variety of industrial processes and consumer products, such as medicines, flavourings, and fragrances.

  6. Ethyl acetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acetate

    Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2. This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops ) and is used in glues , nail polish removers , and the decaffeination process of ...

  7. Phenylacetate - Wikipedia

    en.wikipedia.org/wiki/Phenylacetate

    Phenyl acetate, the ester of phenol and acetic acid; The conjugate base of phenylacetic acid This page was last edited on 14 May 2022, at ...

  8. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    Phenol ethers, similarly to regular ethers, are less hydrophilic than its precursors, phenols and alcohols, both of which can donate and accept hydrogen bonds. Phenol ethers, however, are still able to accept hydrogen bonds through the ethereal oxygen, allowing for its slight solubility in polar solvents.

  9. Phenylacetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Phenylacetaldehyde

    Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers. [1] Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds.