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F13207

Sigma-Aldrich

4-Fluorophenol

99%

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Synonym(s):
4-Hydroxyphenyl fluoride, p-Fluorophenol
Linear Formula:
FC6H4OH
CAS Number:
371-41-5
Molecular Weight:
112.10
Beilstein:
1362752
EC Number:
206-736-0
MDL number:
MFCD00002316
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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M Esseffar et al.
The journal of physical chemistry. A, 113(52), 14711-14717 (2009-10-15)
The interaction of 3,4 dinitrophenol (DNP) with cyclic ketones, lactones, and lactams was investigated by UV-visible spectroscopy and density functional theory (DFT) methods. Equilibrium constants K(HB) for 1:1 hydrogen bonded complexes were determined in solution in CCl(4) and C(6)H(12). For
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
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
Louise C Nolan et al.
Analytical biochemistry, 344(2), 224-231 (2005-08-03)
A spectrophotometric method for the quantitative determination of an enzyme activity resulting in the accumulation of 4-substituted phenols is described in this article. Toluene-4-monooxygenase (T4MO) activity in whole cells of Pseudomonas mendocina KR1 is used to demonstrate this method. This
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