413062
Phenyl trifluoroacetate
97%
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About This Item
Linear Formula:
C6H5CO2CF3
CAS Number:
Molecular Weight:
190.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
207-911-4
MDL number:
Product Name
Phenyl trifluoroacetate, 97%
InChI key
DVCMYAIUSOSIQP-UHFFFAOYSA-N
InChI
1S/C8H5F3O2/c9-8(10,11)7(12)13-6-4-2-1-3-5-6/h1-5H
SMILES string
FC(F)(F)C(=O)Oc1ccccc1
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
127.4 °F - closed cup
flash_point_c
53 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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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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