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339865

Sigma-Aldrich

4-(Trifluoromethoxy)phenol

98%

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About This Item

Linear Formula:
CF3OC6H4OH
CAS Number:
828-27-3
Molecular Weight:
178.11
EC Number:
212-583-0
MDL number:
MFCD00040988
UNSPSC Code:
12352100
PubChem Substance ID:
24860693
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.447 (lit.)

bp

92 °C/25 mmHg (lit.)

density

1.375 g/mL at 25 °C (lit.)

functional group

fluoro

SMILES string

Oc1ccc(OC(F)(F)F)cc1

InChI

1S/C7H5F3O2/c8-7(9,10)12-6-3-1-5(11)2-4-6/h1-4,11H

InChI key

WDRJNKMAZMEYOF-UHFFFAOYSA-N

Application

4-(Trifluoromethoxy)phenol was employed in the catalytic enantioselective synthesis of esters.[1]

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301,H314,H412

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

Flash Point(F)

186.8 °F - closed cup

Flash Point(C)

86 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC1745
BCBZ3591
BCBV9817
WXBC1612V
BCBQ8754V

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Sheryl L Wiskur et al.
Journal of the American Chemical Society, 127(17), 6176-6177 (2005-04-28)
By building on elementary principles of Brønsted acid-base chemistry, a nucleophile-catalyzed method for the asymmetric synthesis of esters from ketenes has been transformed into a much more versatile and effective Brønsted acid-catalyzed process. The product aryl esters can be converted
Kun Qian et al.
Dalton transactions (Cambridge, England : 2003), 47(36), 12759-12768 (2018-08-29)
Dielectric polymer-based nanocomposites have attracted significant attention in recent years for energy storage applications because of their potential high permittivity and breakdown strength. The coupling effect of a nanofiller/matrix interface plays a crucial role in the dielectric and electric properties

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