F13207
4-Fluorophenol
99%
Synonym(s):
4-Hydroxyphenyl fluoride, p-Fluorophenol
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About This Item
Linear Formula:
FC6H4OH
CAS Number:
Molecular Weight:
112.10
Beilstein:
1362752
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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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Signal Word
Warning
Hazard Statements
Precautionary Statements
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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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 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
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
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
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