Molecular structure of Phenyl acetate, CAS Number: 122-79-2
Phenyl acetate (CAS 122-79-2)
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Alternate Names:
Acetic acid phenyl ester
Application:
Phenyl acetate is a useful synthesis reagent and intermediate
CAS Number:
122-79-2
Purity:
≥98%
Molecular Weight:
136.15
Molecular Formula:
C8H8O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Phenyl acetate exhibits is a colorless liquid. It is a synthetic compound comprising phenyl and acetate groups. In the domain of scientific research, Phenyl acetate finds diverse applications. It contributes to the exploration of molecular structure and reactivity, enabling the measurement of compound solubility. Additionally, it aids in the investigation of optical and electrical properties of materials, as well as the examination of molecular interactions.
Phenyl acetate (CAS 122-79-2) References
- Suppression of depleted uranium-induced neoplastic transformation of human cells by the phenyl fatty acid, phenyl acetate: chemoprevention by targeting the p21RAS protein pathway. | Miller, AC., et al. 2001. Radiat Res. 155: 163-170. PMID: 11121229
- A new automated method for phenotyping arylesterase (EC 3.1.1.2) based upon inhibition of enzymatic hydrolysis of 4-nitrophenyl acetate by phenyl acetate. | Haagen, L. and Brock, A. 1992. Eur J Clin Chem Clin Biochem. 30: 391-5. PMID: 1525262
- Reactions of {4-[bis(2-chloroethyl)amino]phenyl}acetic acid (phenylacetic acid mustard) with 2'-deoxyribonucleosides. | Florea-Wang, D., et al. 2007. Chem Biodivers. 4: 406-23. PMID: 17372943
- Temperature dependence of binding and catalysis for human serum arylesterase/paraoxonase. | Debord, J., et al. 2014. Biochimie. 97: 72-7. PMID: 24096087
- Characterization of a versatile arylesterase from Lactobacillus plantarum active on wine esters. | Esteban-Torres, M., et al. 2014. J Agric Food Chem. 62: 5118-25. PMID: 24856385
- Exploring the aryl esterase catalysis of paraoxonase-1 through solvent kinetic isotope effects and phosphonate-based isosteric analogues of the tetrahedral reaction intermediate. | Bavec, A., et al. 2014. Biochimie. 106: 184-6. PMID: 25180809
- Dynamic changes of paraoxonase 1 activity towards paroxon and phenyl acetate during coronary artery surgery. | Wysocka, A., et al. 2017. BMC Cardiovasc Disord. 17: 92. PMID: 28376720
- γ-Cyclodextrin-phenylacetic acid mesh as a drug trap. | Yu, HS., et al. 2018. Carbohydr Polym. 184: 390-400. PMID: 29352934
- Shared strategies for β-lactam catabolism in the soil microbiome. | Crofts, TS., et al. 2018. Nat Chem Biol. 14: 556-564. PMID: 29713061
- An Historical Review of Phenylacetic Acid. | Cook, SD. 2019. Plant Cell Physiol. 60: 243-254. PMID: 30649529
- Exhaled breath analysis using on-line preconcentration mass spectrometry for gastric cancer diagnosis. | Hong, Y., et al. 2021. J Mass Spectrom. 56: e4588. PMID: 32633879
- Steady-state kinetic analysis of human cholinesterases over wide concentration ranges of competing substrates. | Mukhametgalieva, AR., et al. 2022. Biochim Biophys Acta Proteins Proteom. 1870: 140733. PMID: 34662731
- RIFM fragrance ingredient safety assessment, phenylacetic acid, CAS Registry Number 103-82-2. | Api, AM., et al. 2022. Food Chem Toxicol. 167 Suppl 1: 113240. PMID: 35718012
- A biochemical explanation of phenyl acetate neurotoxicity in experimental phenylketonuria. | Loo, YH., et al. 1985. J Neurochem. 45: 1596-600. PMID: 4045466
- Urinary phenyl acetate: a diagnostic test for depression? | Sabelli, HC., et al. 1983. Science. 220: 1187-8. PMID: 6857245
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ASL.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Phenyl acetate, 5 g | sc-250690 | 5 g | $30.00 |