178470
4-(Trifluoromethyl)phenol
97%
Synonym(s):
α,α,α-Trifluoro-p-cresol, 4-Hydroxybenzotrifluoride
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About This Item
Linear Formula:
CF3C6H4OH
CAS Number:
Molecular Weight:
162.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-945-7
Beilstein/REAXYS Number:
1637019
MDL number:
Assay:
97%
Form:
liquid
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
Related Categories
General description
4-(Trifluoromethyl)phenol molecule, bound at the active site of H61T (His-61→Thr) mutant, shows strong density.
4-(Trifluoromethyl)phenol also known as p-trifluoromethylphenol, is used in synthesis of polymers and monomers.
4-(Trifluoromethyl)phenol also known as p-trifluoromethylphenol, is used in synthesis of polymers and monomers.
Application
4-(Trifluoromethyl)phenol (4-hydroxybenzotrifluoride) was used in the synthesis of diaryl ether.
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
Storage Class
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
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Selina Tisler et al.
Environmental science & technology, 53(13), 7400-7409 (2019-05-29)
The present study investigates the transformation of the antidepressant fluoxetine (FLX) by photo- and biodegradation and shows similarities and differences in transformation products (TPs). TPs were identified using LC-high-resolution mass spectrometry with positive and negative electrospray ionization. In a sunlight
D C Thompson et al.
Chemico-biological interactions, 126(1), 1-14 (2000-05-29)
4-Trifluoromethylphenol (4-TFMP) was cytotoxic to precision-cut rat liver slices as indicated by loss of intracellular potassium. Intracellular glutathione levels decreased and fluoride ion levels increased in a time and concentration-dependent manner. The cytotoxicity of 4-TFMP did not appear to be
Synthesis of Poly-p-oxyperfluorobenzylene and Related Polymers. A Novel Synthesis of the Monomer 2, 3, 5, 6-Tetrafluoro-4-trifluoromethylphenol
Journal of Research of the National Bureau of Standards, 71, 33-33 (1967)
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
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
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