122726
4-Acetylbiphenyl
98%
Synonym(s):
4-Biphenyl methyl ketone, 4-Phenylacetophenone
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About This Item
Linear Formula:
C6H5C6H4COCH3
CAS Number:
Molecular Weight:
196.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-202-6
Beilstein/REAXYS Number:
1101615
MDL number:
Assay:
98%
InChI
1S/C14H12O/c1-11(15)12-7-9-14(10-8-12)13-5-3-2-4-6-13/h2-10H,1H3
InChI key
QCZZSANNLWPGEA-UHFFFAOYSA-N
SMILES string
CC(=O)c1ccc(cc1)-c2ccccc2
assay
98%
mp
116-118 °C (lit.)
solubility
chloroform: soluble 10mg/200microlitres, clear, colorless to faintly yellow
Quality Level
Application
4-Acetylbiphenyl was used to study the inactivation of 7-ethoxy-4-trifluoromethylcoumarin O-deethylase activity by various arylalkynes. It may be used in the synthesis of Schiffs base.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 2
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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E S Roberts et al.
Drug metabolism and disposition: the biological fate of chemicals, 25(11), 1242-1248 (1997-11-14)
The time-dependent loss of the 7-ethoxy-4-trifluoromethylcoumarin (EFC) O-deethylase activity of rat P450 2B1, rabbit P450 2B4, or dog P450 2B11 by 1-ethynylnaphthalene (1EN), 2-ethynylnaphthalene (2EN), 2-(1-propynyl)naphthalene (2PN), 1-ethynylanthracene (1EA), 2-ethynylanthracene, 2-ethynylphenanthrene, 3-ethynylphenanthrene, 9-ethynylphenanthrene (9EPh), 9-(1-propynyl)phenanthrene (9PPh), 4-ethynylpyrene (4EP), and 4-(1-propynyl)biphenyl
Synthesis, Characterization and Antifungal Activity of Some Transition Metal Complexes of the Schiff Base Derived from 4-Acetylbi-Phenyl and S-Benzyldithiocarbazate.
Bi S and Li G.
Synth. React. Inorg. Met.-Org. Chem. , 29(10), 1829-1841 (1999)
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