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413062

Sigma-Aldrich

Phenyl trifluoroacetate

97%

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About This Item

Linear Formula:
C6H5CO2CF3
CAS Number:
500-73-2
Molecular Weight:
190.12
EC Number:
207-911-4
MDL number:
MFCD00039232
UNSPSC Code:
12352100
PubChem Substance ID:
24865841
NACRES:
NA.22
form:
liquid
Assay:
97%

Assay

97%

form

liquid

refractive index

n20/D 1.419 (lit.)

bp

146-147 °C (lit.)

density

1.276 g/mL at 25 °C (lit.)

functional group

ester
fluoro
phenoxy

SMILES string

FC(F)(F)C(=O)Oc1ccccc1

InChI

1S/C8H5F3O2/c9-8(10,11)7(12)13-6-4-2-1-3-5-6/h1-5H

InChI key

DVCMYAIUSOSIQP-UHFFFAOYSA-N

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

127.4 °F - closed cup

Flash Point(C)

53 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV0192
MKCP2904
MKCF7516
MKCD8253
MKBZ3981V

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Kinetics and mechanisms of reactions of pyridines and imidazoles with phenyl acetates and trifluoroacetates in aqueous acetonitrile with low content of water: nucleophilic and general base catalysis in ester hydrolysis.
Neuvonen H.
J. Chem. Soc. Perkin Trans. II, 2(2), 159-167 (1987)
pH Dependent effect of ?-cyclodextrin on the hydrolysis rate of trifluoroacetate esters.
Fernandez MA, et al.
The Journal of Organic Chemistry, 62(2), 7554-7559 (1997)
1, 4-Addition of arylboronic acids and arylsiloxanes to a, ?-unsaturated carbonyl compounds via transmetalation to dicationic palladium (II) complexes.
Nishikata T, et al.
Organometallics, 23(18), 4317-4324 (2004)
Synthesis, characterization, and copolymerization of a series of novel acid monomers based on sulfonimides for proton conducting membranes.
Rahman MK, et al.
Macromolecules, 37(15), 5572-5577 (2004)

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