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Merck
CN

F13207

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24894759
EC Number:
206-736-0
Beilstein/REAXYS Number:
1362752
MDL number:
MFCD00002316

Key Documents

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Product Name

4-Fluorophenol, 99%

InChI key

RHMPLDJJXGPMEX-UHFFFAOYSA-N

InChI

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

SMILES string

Oc1ccc(F)cc1

assay

99%

bp

185 °C (lit.)

mp

43-46 °C (lit.)

Quality Level

100

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GHS07

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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

11 - Combustible Solids

wgk

WGK 1

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN5734
BCCN0962
BCCM6680
BCCK4663
BCCJ3497

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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
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
Lydie Coulombel et al.
Applied microbiology and biotechnology, 89(6), 1867-1875 (2010-11-09)
Escherichia coli cells, expressing 4-hydroxyphenylacetate 3-hydroxylase, fully transformed 4-halogenated phenols to their equivalent catechols as single products in shaken flasks. 4-Fluorophenol was transformed at a rate 1.6, 1.8, and 3.4-fold higher than the biotransformation of 4-chloro-, 4-bromo-, and 4-iodo-phenol, respectively.
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
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
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