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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).
It's also used in the illicit production of phenylacetone, which is used in the manufacture of methamphetamine. The sodium salt of phenylacetic acid, sodium phenylacetate, is used as a pharmaceutical drug for the treatment of urea cycle disorders , including as the combination drug sodium phenylacetate/sodium benzoate (Ammonul).
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 21:52 (UTC). Text is ...
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.
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.
Amyl acetate (pentyl acetate) is an organic compound and an ester with the chemical formula CH 3 COO[CH 2] 4 CH 3 and the molecular weight 130.19 g/mol. It is colorless and has a scent similar to bananas [3] [4] and apples. [5] The compound is the condensation product of acetic acid and 1-pentanol.
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.
It adopts a T-shaped molecular geometry, with the phenyl group occupying one of the three equatorial positions of a trigonal bipyramid (lone pairs occupy the other two) and the axial positions occupied by oxygen atoms from the acetate groups. The "T" is distorted in that the phenyl-C to I to acetate-O bond angles are less than 90°. [1]