F13207
4-氟苯酚
99%
别名:
4-氟苯酚, 对氟苯酚
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关于此项目
线性分子式:
FC6H4OH
化学文摘社编号:
分子量:
112.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-736-0
Beilstein/REAXYS Number:
1362752
MDL number:
产品名称
4-氟苯酚, 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
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signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2
存储类别
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
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.
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
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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