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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).
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. Endogenously, it is a catabolite of phenylalanine.
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. Methyl phenylacetate has a strong odor similar to honey.
Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is an alpha-CH2-containing aldehyde and a member of ...
Chemical formula. C 8 H 8 O 3: Molar mass: 152.149 g·mol −1 Appearance Beige powder Melting point: 150 °C (302 °F; 423 K) Hazards Safety data sheet (SDS)
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.
The enzyme acetylacetone dioxygenase cleaves a central carbon-carbon bond of acetylacetone, producing acetate and 2-oxopropanal. The enzyme is iron(II)-dependent, but it has been proven to bind to zinc as well. Acetylacetone degradation has been characterized in the bacterium Acinetobacter johnsonii. [13] CH 3 C(O)CH 2 C(O)CH 3 + O 2 → CH 3 ...