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102741

Sigma-Aldrich

2-Fluorbiphenyl

96%

Synonym(e):

1-Fluoro-2-phenylbenzene, o-Fluorodiphenyl

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About This Item

Lineare Formel:
C6H5C6H4F
CAS-Nummer:
321-60-8
Molekulargewicht:
172.20
Beilstein:
2043175
EG-Nummer:
206-290-7
MDL-Nummer:
MFCD00000317
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24846587
NACRES:
NA.22

Qualitätsniveau

100

Assay

96%

Form

solid

bp

248 °C (lit.)

mp (Schmelzpunkt)

71-74 °C (lit.)

Funktionelle Gruppe

fluoro
phenyl

SMILES String

Fc1ccccc1-c2ccccc2

InChI

1S/C12H9F/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H

InChIKey

KLECYOQFQXJYBC-UHFFFAOYSA-N

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Allgemeine Beschreibung

2-Fluorobiphenyl is a white to off white powder. It is catabolized by C. elegans, yielding hydroxylated products. The metabolism of 2-fluorobiphenyl by hepatic microsomes isolated from control and aroclor 1254-treated rats and pigeons was studied.

Anwendung

2-Fluorobiphenyl was used as an internal standard for analysis of environmental pollutants in sediments using pressurized liquid extraction and gas chromatography-mass spectrometry. It was used to study the solvent dynamics of 1,2,4,5-tetracyanobenzene/biphenyl derivative radical ion pairs by picosecond absorption spectroscopy. It was also used as a sole carbon and energy source for the biphenyl-degrading bacterium Pseudomonas pseudoalcaligenes KF707.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

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Analysenzertifikate (COA)

Lot/Batch Number
0000303864
0000303864
MKCT8083
0000247169
0000255602

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Cormac D Murphy et al.
FEMS microbiology letters, 286(1), 45-49 (2008-07-12)
The biphenyl-degrading bacterium Pseudomonas pseudoalcaligenes KF707 can use 2- and 4-fluorobiphenyl as sole carbon and energy sources. Accumulation of fluorinated catabolites was determined by fluorine-19 nuclear magnetic spectroscopy (19F NMR) and revealed that growth on 4-fluorobiphenyl yielded 4-fluorobenzoate and 4-fluoro-1,2-dihydro-1,2-dihydroxybenzoate
Jessica Amadio et al.
Applied microbiology and biotechnology, 86(1), 345-351 (2009-12-04)
The fungus Cunninghamella elegans is a useful model of human catabolism of xenobiotics. In this paper, the biotransformation of fluorinated biphenyls by C. elegans was investigated by analysis of the culture supernatants with a variety of analytical techniques. 4-Fluorobiphenyl was
Solvent Effect on the Dynamics of Radical Ion Pair Separation.
Han CH.
Journal of Photoscience, 8(1), 33-37 (2001)
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Fine roots of woody plants are a heterogeneous system differing markedly in structure and function. Nevertheless, knowledge about the plant uptake of organic pollutants via fine roots is scarce to date. In the present study, plant uptake, translocation, and return
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