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F13207

Sigma-Aldrich

4-Fluorophenol

99%

Synonym(s):

4-Hydroxyphenyl fluoride, p-Fluorophenol

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About This Item

Linear Formula:
FC6H4OH
CAS Number:
371-41-5
Molecular Weight:
112.10
Beilstein:
1362752
EC Number:
206-736-0
MDL number:
MFCD00002316
UNSPSC Code:
12352100
PubChem Substance ID:
24894759
NACRES:
NA.22

Assay

99%

bp

185 °C (lit.)

mp

43-46 °C (lit.)

SMILES string

Oc1ccc(F)cc1

InChI

1S/C6H5FO/c7-5-1-3-6(8)4-2-5/h1-4,8H

InChI key

RHMPLDJJXGPMEX-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

154.4 °F - closed cup

Flash Point(C)

68 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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A M Osman et al.
Chemico-biological interactions, 104(2-3), 147-164 (1997-05-02)
The present study shows that MP8 in the presence of H2O2 is able to catalyze the rupture of the stable carbon-fluorine bond of 4-fluorophenol, used as a model substrate for the oxidative dehalogenation reaction. 1,4-Benzoquinone was shown to be the
Manfred Lehnig et al.
Organic & biomolecular chemistry, 4(4), 721-729 (2006-02-10)
Peroxynitric acid (O2NOOH) nitrates L-tyrosine and related compounds at pH 2-5. During reaction with O2(15)NOOH in the probe of a 15N NMR spectrometer, the NMR signals of the nitration products of L-tyrosine, N-acetyl-L-tyrosine, 4-fluorophenol and 4-methoxyphenylacetic acid appear in emission
Alexandria Harkey et al.
Biotechnology letters, 34(9), 1725-1731 (2012-05-29)
Cytochrome P450(BM3)-F87G catalyzed the oxidative defluorination of 4-fluorophenol, followed by reduction of the resulting benzoquinone to hydroquinone via the NADPH P450-reductase activity of the enzyme. The k (cat) and K (m) for this reaction were 71 ± 5 min(-1) and
Maria Isabel M Ferreira et al.
Applied and environmental microbiology, 75(24), 7767-7773 (2009-10-20)
Arthrobacter sp. strain IF1 is able to grow on 4-fluorophenol (4-FP) as a sole source of carbon and energy. To clone the 4-FP degradation genes, DNA libraries were constructed and screened with a probe obtained by PCR using primers designed
Tobias L Ross et al.
Molecules (Basel, Switzerland), 16(9), 7621-7626 (2011-09-09)
4-[(18)F]Fluorophenol is a versatile synthon for the synthesis of more complex radiopharmaceuticals bearing a 4-[(18)F]fluorophenoxy moiety. In order to prepare 4-[(18)F]fluorophenol in no-carrier-added (n.c.a.) form only a nucleophilic labelling method starting from [(18)F]fluoride is suitable. In this paper a new
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