| Weight | 136.15 g/mol |
|---|---|
| Formula | C8H8O2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
PHENYLACETIC ACID (103-82-2)
phenylacetate · sodium phenylacetate · phenylacetic acid, sodium salt , carboxy-(11)C-labeled cpd
Score:
#1368 in Biology
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#1601 in Chemistry
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- Lovastatin and phenylacetate inhibit the induction of nitric oxide synthase and cytokines in rat primary astrocytes, microglia, and macrophages. (Journal of Clinical Investigation, 1997)
- Survival after treatment with phenylacetate and benzoate for urea-cycle disorders. (The New England Journal of Medicine, 2007)
- Molecular characterization of the phenylacetic acid catabolic pathway in Pseudomonas putida U: The phenylacetyl-CoA catabolon (Proceedings of the National Academy of Sciences of the United States of America, 1998)
- Catabolism of Phenylacetic Acid in Escherichia coli CHARACTERIZATION OF A NEW AEROBIC HYBRID PATHWAY (Journal of Biological Chemistry, 1998)
- Purification and biochemical characterization of phenylacetyl-CoA ligase from Pseudomonas putida. A specific enzyme for the catabolism of phenylacetic acid. (Journal of Biological Chemistry, 1990)
- Phenylacetate: A Novel Nontoxic Inducer of Tumor Cell Differentiation (Cancer Research, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phenylacetate
- sodium phenylacetate
- phenylacetic acid, sodium salt , carboxy-(11)C-labeled cpd
- phenylacetic acid, potassium salt
- phenylacetic acid, cesium salt
- phenylacetic acid, sodium salt
- phenylacetic acid, lithium salt
- phenylacetic acid, rubidium salt
- phenylacetic acid, mercury salt
- phenylacetic acid, ammonium salt
- phenylacetic acid, calcium salt
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SMILESC1=CC=C(C=C1)CC(=O)O
-
InChIKeyWLJVXDMOQOGPHL-UHFFFAOYSA-N
- Pubchem - PHENYLACETIC ACID
- Wikipedia - phenylacetic acid
Phenylacetic acid (PAA) (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 disagreeable odor. Endogeneously, it is a catabolite of phenylalanine.
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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