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Key Documents

396451

Sigma-Aldrich

4-[4-(Trifluoromethyl)phenoxy]phenol

98%

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About This Item

Linear Formula:
CF3C6H4OC6H4OH
CAS Number:
Molecular Weight:
254.20
Beilstein/REAXYS Number:
2055876
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

mp

49-54 °C (lit.)

functional group

fluoro

SMILES string

Oc1ccc(Oc2ccc(cc2)C(F)(F)F)cc1

InChI

1S/C13H9F3O2/c14-13(15,16)9-1-5-11(6-2-9)18-12-7-3-10(17)4-8-12/h1-8,17H

InChI key

FJFSSESWAFPCSU-UHFFFAOYSA-N

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signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Erik R Christensen et al.
Environmental toxicology and chemistry, 28(4), 826-835 (2009-04-28)
We derive equations for the effective concentration giving 10% inhibition (EC10) with 95% confidence limits for probit (log-normal), Weibull, and logistic dose-response models on the basis of experimentally derived median effective concentrations (EC50s) and the curve slope at the central
Tukayi Kudanga et al.
Bioresource technology, 101(8), 2793-2799 (2010-01-02)
This work presents for the first time the mechanistic evidence of a laccase-catalyzed method of covalently grafting hydrophobicity enhancing fluorophenols onto Fagus sylvatica veneers. Coupling of fluorophenols onto complex lignin model compounds guaiacylglycerol beta-guaiacyl ether and syringylglycerol beta-guaiacyl ether was

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