Ethyl phenylacetate

The Ethyl phenylacetate with the cas number 101-97-3, is also called (1) Acetic acid, phenyl-, ethyl ester ; (2) Benzeneacetic acid, ethyl ester ; (3) Ethyl 2-phenylethanoate ; (4) Ethyl alpha-toluate ; (5) Ethyl benzeneacetate ; (6) Ethyl phenacetate ; (7) Ethyl phenylacetate ; (8) Ethyl phenylethanoate ; (9) Phenylacetic acid, ethyl ester ; (10) UNII-V6CNZ04D8O ; (11) alpha-Toluic acid, ethyl ester. Ethyl phenylacetate belongs to the following Product Categories: (1)Pharmaceutical Intermediates; (2)Organics;API intermediates; (3)C10 to C11; (4)Carbonyl Compounds; (5)Esters;Alphabetical Listings; (6)Flavors and Fragrances and so on.

Properties of Ethyl phenylacetate: (1)H bond acceptors: 2 ; (2)H bond donors: 0 ; (3)Freely Rotating Bonds: 4 ; (4)Polar Surface Area: 26.3 Å² ; (5)Index of Refraction: 1.501 ; (6) Molar Refractivity: 46.84 cm³ ; (7)Molar Volume: 158.7 cm³ ; (8)Polarizability: 18.56×10^-24cm³ ; (9)Surface Tension: 35.7 dyne/cm ; (10) Density: 1.034 g/cm³ ; (11)Flash Point: 98.2 °C ; (12)Enthalpy of Vaporization: 46.13 kJ/mol ; (13)Boiling Point: 224.8 °C at 760 mmHg ; (14)Vapour Pressure: 0.0897 mmHg at 25°C

Uses of Ethyl phenylacetate: Mycophenolate mofetil seems like clear colourless to pale yellowish liquid with a pleasant smell. Miscibility of ethanol, ethyl ether, benzene and chloroform but insoluble in water. Ethyl phenylacetate is used as synthetic spices, which is mainly used for spices in cigarettes, soap and make ups. Further more, it is slightly used for spices of flores aurantii and baked bean.
When you are using Ethyl phenylacetate, please be cautious about it. Do not breathe vapour and avoid contact with skin and eyes.

Production of Ethyl phenylacetate: Ethyl phenylacetate can be produced by three method:
Firstly, Ethyl phenylacetate can be produced by reflux reaction of the benzene acetonitrile, ethanol and sulphuric acid . Secondly, Ethyl phenylacetate can also manufactured by esterification of the benzene acetic acid and ethanol under the effect of sulfuric acid. Yield is 90%. Thirdly, another production method is that esterification and hydrolyzation of Phenylacetamide to obtain Ethyl phenylacetate.

You can still convert the following datas into molecular structure :
1.SMILES: O=C(Cc1ccccc1)OCC
2. InChI: InChI=1/C10H12O2/c1-2-12-10(11)8-9-6-4-3-5-7-9/h3-7H,2,8H2,1H3

Ethyl phenylacetate toxic data can be showed in the following sheet.