178470
4-(三氟甲基)苯酚
97%
别名:
α,α,α-三氟对甲酚, 对三氟甲基苯酚
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关于此项目
线性分子式:
CF3C6H4OH
化学文摘社编号:
分子量:
162.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-945-7
Beilstein/REAXYS Number:
1637019
MDL number:
产品名称
4-(三氟甲基)苯酚, 97%
InChI key
BAYGVMXZJBFEMB-UHFFFAOYSA-N
InChI
1S/C7H5F3O/c8-7(9,10)5-1-3-6(11)4-2-5/h1-4,11H
SMILES string
Oc1ccc(cc1)C(F)(F)F
assay
97%
form
liquid
mp
45-47 °C (lit.)
functional group
fluoro
storage temp.
2-8°C
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Application
4-（三氟甲基）苯酚（4- hydroxybenzotrifluoride）被用于二芳基醚的合成。
General description
4-（三氟甲基）苯酚分子，与 H61T（HIS-61→苏氨酸）突变体的活性位点结合，密度较强。
4-（三氟甲基）苯酚又称p-三氟甲基苯酚，用于合成聚合物和单体。
4-（三氟甲基）苯酚又称p-三氟甲基苯酚，用于合成聚合物和单体。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
4.1B - Flammable solid hazardous materials
wgk
WGK 3
flash_point_f
183.2 °F - closed cup
flash_point_c
84 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
B van de Wier et al.
Chemico-biological interactions, 242, 139-144 (2015-10-03)
Cytochrome P450 2E1 (CYP2E1) expression and activity in the liver is associated with the degree of liver damage in patients with alcoholic steatohepatitis (ASH) as well as non-alcoholic steatohepatitis (NASH). CYP2E1 is known to generate reactive oxygen species, which leads
Jin-Kyun Lee et al.
Chemical communications (Cambridge, England), (39)(39), 4780-4782 (2008-10-03)
A high yielding, batch mode synthesis of diaryl ethers and sulfides by an S(N)Ar fluoride-mediated process in scCO(2) has been developed; the use of a polymer-supported imidazolium fluoride reagent in batch mode led to the development of a fixed-bed continuous
M W Fraaije et al.
The Journal of biological chemistry, 275(49), 38654-38658 (2000-09-14)
Vanillyl-alcohol oxidase (VAO) is member of a newly recognized flavoprotein family of structurally related oxidoreductases. The enzyme contains a covalently linked FAD cofactor. To study the mechanism of flavinylation we have created a design point mutation (His-61 --> Thr). In
Lisa Bauer et al.
ACS infectious diseases, 5(9), 1609-1623 (2019-07-16)
Enteroviruses (family Picornaviridae) comprise a large group of human pathogens against which no licensed antiviral therapy exists. Drug-repurposing screens uncovered the FDA-approved drug fluoxetine as a replication inhibitor of enterovirus B and D species. Fluoxetine likely targets the nonstructural viral
L J Urichuk et al.
Journal of chromatography. B, Biomedical sciences and applications, 698(1-2), 103-109 (1997-11-21)
An electron-capture gas chromatographic procedure was developed for the analysis of p-trifluoromethylphenol, an O-dealkylated metabolite of fluoxetine, in biological samples. A basic extraction of the biological sample was employed, followed by derivatization with pentafluorobenzenesulfonyl chloride. The internal standard, 2,4-dichlorophenol, was
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