质量水平
方案
99%
沸点
185 °C (lit.)
mp
43-46 °C (lit.)
SMILES字符串
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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警示用语：
Warning
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
154.4 °F - closed cup
闪点(°C)
68 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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
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
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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