440078
Phenyl phenylacetate
96%
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About This Item
Linear Formula:
C6H5CH2CO2C6H5
CAS Number:
Molecular Weight:
212.24
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Assay:
96%
Form:
solid
InChI
1S/C14H12O2/c15-14(11-12-7-3-1-4-8-12)16-13-9-5-2-6-10-13/h1-10H,11H2
SMILES string
O=C(Cc1ccccc1)Oc2ccccc2
InChI key
USVNNHYNCCJCCP-UHFFFAOYSA-N
assay
96%
form
solid
bp
158 °C/7 mmHg (lit.)
mp
40-42 °C (lit.)
Gene Information
human ... EPHX2(2053)
mouse ... Ephx2(13850)
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Photochemistry of phenyl phenylacetates adsorbed on pentasil andfaujasite zeolites.
Tung C-H and Ying Y-M.
J. Chem. Soc. Perkin Trans. II, 7, 1319-1322 (1997)
Molecular rearrangements. Part XX. Thermolysis of carboxylic acid esters.
Aly MM, et al.
Canadian Journal of Chemistry, 61(7), 1532-1535 (1983)
C D Carrington et al.
The Biochemical journal, 236(2), 503-507 (1986-06-01)
For the purpose of assessing the neurotoxic potential of organophosphorus compounds, it has been determined that paraoxon-preinhibited hen brain has both neurotoxicant (mipafox)-sensitive (neurotoxic esterase; NTE) and -insensitive esterase components. Several experiments designed to investigate the kinetic parameters governing the
Selectivity in the photo-Fries reaction of phenyl phenylacetates included in a Nafion membrane.
Tung C-H and Xu X-H.
Tetrahedron Letters, 40(1), 127-130 (1999)
L Haagen et al.
European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies, 30(7), 391-395 (1992-07-01)
A new method for phenotyping human serum arylesterase (EC 3.1.1.2) is described and evaluated. The aromatic esters, phenyl acetate and 4-nitrophenyl acetate, were compared as substrates for spectrophotometric measurement of arylesterase activity. A method for arylesterase phenotyping, based upon inhibition
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