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122726

Sigma-Aldrich

4-Acetylbiphenyl

98%

Synonym(s):

4-Biphenyl methyl ketone, 4-Phenylacetophenone

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About This Item

Linear Formula:
C6H5C6H4COCH3
CAS Number:
92-91-1
Molecular Weight:
196.24
Beilstein/REAXYS Number:
1101615
EC Number:
202-202-6
MDL number:
MFCD00008749
UNSPSC Code:
12352100
PubChem Substance ID:
24847504
NACRES:
NA.22

Quality Level

100

assay

98%

mp

116-118 °C (lit.)

solubility

chloroform: soluble 10mg/200microlitres, clear, colorless to faintly yellow

SMILES string

CC(=O)c1ccc(cc1)-c2ccccc2

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

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Application

4-Acetylbiphenyl was used to study the inactivation of 7-ethoxy-4-trifluoromethylcoumarin O-deethylase activity by various arylalkynes[1]. It may be used in the synthesis of Schiffs base[2].

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR3221
MKCL4471
MKCD2660
MKCD1166
MKBV2879V

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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)
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

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