p-Trifluoromethoxy phenol

Modify Date: 2024-01-02 16:12:17

p-Trifluoromethoxy phenol Structure
p-Trifluoromethoxy phenol structure
Common Name p-Trifluoromethoxy phenol
CAS Number 828-27-3 Molecular Weight 178.109
Density 1.4±0.1 g/cm3 Boiling Point 187.5±0.0 °C at 760 mmHg
Molecular Formula C7H5F3O2 Melting Point 17-18°C
MSDS Chinese USA Flash Point 86.1±0.0 °C
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name 4-(Trifluoromethoxy)phenol
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 187.5±0.0 °C at 760 mmHg
Melting Point 17-18°C
Molecular Formula C7H5F3O2
Molecular Weight 178.109
Flash Point 86.1±0.0 °C
Exact Mass 178.024170
PSA 29.46000
LogP 2.35
Vapour Pressure 0.5±0.3 mmHg at 25°C
Index of Refraction 1.462

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302-H312-H315-H319-H332-H335
Precautionary Statements P261-P280-P305 + P351 + P338
Personal Protective Equipment Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xn:Harmful;
Risk Phrases R20/21/22;R36/37/38
Safety Phrases S26-S27-S36/37/39
RIDADR 2927
WGK Germany 2
Packaging Group III
Hazard Class 6.1
HS Code 29095090

 Customs

HS Code 2909500000
Summary 2909500000 ether-phenols, ether-alcohol-phenols and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

 Articles1

More Articles
Catalytic asymmetric synthesis of esters from ketenes.

J. Am. Chem. Soc. 127(17) , 6176-7, (2005)

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...

 Synonyms

Phenol, 4-(trifluoromethoxy)-
p-(Trifluoromethoxy)phenol
QR DOXFFF
EINECS 212-583-0
p-Trifluoromethoxy phenol
α,α,α,4-Tetrafluoroanisole
MFCD00040988
4-(Trifluoromethoxy)phenol
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