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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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Maria Isabel M Ferreira et al.
Applied microbiology and biotechnology, 78(4), 709-717 (2008-01-30)
A Gram-positive bacterial strain capable of aerobic biodegradation of 4-fluorophenol (4-FP) as the sole source of carbon and energy was isolated by selective enrichment from soil samples collected near an industrial site. The organism, designated strain IF1, was identified as
Augusto Rivera et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 74(2), 588-590 (2009-08-21)
The proton affinity scale of small aminal cages was investigated using experimental and theoretical methodologies. The formation constant (K(f)) was determined for 1:1 hydrogen-bonded complexes between p-fluorophenol (PFP) and some aminal cage type (B) in CCl(4) at 298 K using
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
Thomas Ludwig et al.
Nuclear medicine and biology, 29(2), 255-262 (2002-02-02)
This paper describes the improved synthesis of n.c.a. 4- 18F]fluorophenol for the preparation of 18F-labeled alkylarylethers. Nucleophilic fluorination of substituted benzophenone derivatives yielded n.c.a. 4- 18F]fluoro-4'-substituted benzophenones with 80- 90% RCY, which were converted to benzoic acid phenylesters by treatment
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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