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108723

Sigma-Aldrich

Phenyl acetate

99%

Synonyme(s) :

Acetic acid phenyl ester

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About This Item

Formule linéaire :
CH3COOC6H5
Numéro CAS:
122-79-2
Poids moléculaire :
136.15
Numéro Beilstein :
636458
Numéro CE :
204-575-0
Numéro MDL:
MFCD00008699
Code UNSPSC :
12352100
ID de substance PubChem :
24846821
Nomenclature NACRES :
NA.22

Niveau de qualité

100

Pureté

99%

Indice de réfraction

n20/D 1.501 (lit.)

Point d'ébullition

196 °C (lit.)

Densité

1.073 g/mL at 25 °C (lit.)

Groupe fonctionnel

ester
phenoxy

Chaîne SMILES 

CC(=O)Oc1ccccc1

InChI

1S/C8H8O2/c1-7(9)10-8-5-3-2-4-6-8/h2-6H,1H3

Clé InChI

IPBVNPXQWQGGJP-UHFFFAOYSA-N

Informations sur le gène

human ... PON1(5444)

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Catégories apparentées

Description générale

Phenyl acetate is an aromatic ester. Phenyl acetate levels in urine are marker for the diagnosis of some forms of unipolar major depressive disorders. It undergoes Fries rearrangement to form a mixture of o- and p-hydroxyacetophenones which are useful intermediates in manufacture of pharmaceuticals.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

170.6 °F - closed cup

Point d'éclair (°C)

77 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificats d'analyse (COA)

Lot/Batch Number
MKBN8367V
05511CJ
03208JF
14827CI
05708PN

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Consulter la Bibliothèque de documents

Ferhat Içme et al.
Turkish journal of medical sciences, 45(4), 947-953 (2015-10-02)
The aims of this study were to investigate the significance of oxidative stress parameters in the pathogenesis of ischemic stroke and hemorrhagic stroke and to investigate their effects on stroke severity using the National Institutes of Health Stroke Scale (NIHSS).
Cristiano Noto et al.
Journal of psychiatric research, 68, 210-216 (2015-08-01)
Schizophrenia is accompanied by increased lipid peroxidation and nitric oxide (NO) levels and by lowered antioxidant levels. However, the effect of antipsychotic agents on these processes remains unclear. The objective of this study is to determine the oxidative stress (OS)
Chang Li et al.
Scientific reports, 9(1), 5979-5979 (2019-04-14)
High-density lipoprotein (HDL) confers protection against cardiovascular disease partly attributable to its robust anti-oxidant activities, which is largely impaired in diabetic conditions. In this study, we analyzed the anti-oxidant activity of HDL, as represented by the arylesterase activity of paraoxonase
Solvent effects in liquid phase Fries rearrangement of phenyl acetate over a HBEA zeolite.
Jayat F, et al.
Catalysis Letters, 41(3-4), 181-187 (1996)
Vasilios Hatzistavros et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 21(7), 823-826 (2005-07-26)
Selective membranes containing a few micrograms of various complexing reagents in a polyvinyl chloride (PVC) matrix were produced in order to determine low uranium concentrations in water. The membranes were produced on the surfaces of quartz glasses, and immersed in
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Articles

Fries Rearrangement

The Fries rearrangement reaction is an organic name reaction which involves the conversion of phenolic esters into hydroxyaryl ketones on heating in the presence of a catalyst. Suitable catalysts for this reaction are Brønsted or Lewis acids such as HF, AlCl3, BF3, TiCl4, or SnCl4. The Fries rearrangement reaction is an ortho, para-selective reaction, and is used in the preparation of acyl phenols. This organic reaction has been named after German chemist Karl Theophil Fries.

Fries Rearrangement

The Fries rearrangement reaction is an organic name reaction which involves the conversion of phenolic esters into hydroxyaryl ketones on heating in the presence of a catalyst. Suitable catalysts for this reaction are Brønsted or Lewis acids such as HF, AlCl3, BF3, TiCl4, or SnCl4. The Fries rearrangement reaction is an ortho, para-selective reaction, and is used in the preparation of acyl phenols. This organic reaction has been named after German chemist Karl Theophil Fries.

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