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Merck
CN

101893

Perfluorobenzophenone

98%

Synonym(s):

Decafluorobenzophenone, Perfluorobenzophenone

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About This Item

Linear Formula:
C6F5COC6F5
CAS Number:
Molecular Weight:
362.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-717-8
Beilstein/REAXYS Number:
2066476
MDL number:
Assay:
98%
Form:
solid
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Quality Level

assay

98%

form

solid

mp

90-95 °C (lit.)

SMILES string

Fc1c(F)c(F)c(c(F)c1F)C(=O)c2c(F)c(F)c(F)c(F)c2F

InChI

1S/C13F10O/c14-3-1(4(15)8(19)11(22)7(3)18)13(24)2-5(16)9(20)12(23)10(21)6(2)17

InChI key

WWQLXRAKBJVNCC-UHFFFAOYSA-N

Application

Perfluorobenzophenone was used in the synthesis of fluorinated acridones and acridines.

Biochem/physiol Actions

Perfluorobenzophenone alcoholic solution generates ketyl and radical anion which can be studied by electron spin resonance spectra. Perfluorobenzophenone undergoes photolysis to form ketyl (C6F5)C.OH radical.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Orthogonal Synthesis of Fluorinated Acridones and Acridines from Perfluorobenzophenone.
Del Buttero P, et al
European Journal of Organic Chemistry, 2011(12), 2265-2271 (2011)
The Electron Spin Resonance Spectra of the Photochemically Produced Perfluorobenzophenone Ketyl and Anion Radicals.
Sargent FP and Bailey MG.
Canadian Journal of Chemistry, 49(13), 2350-2352 (1971)
The Photochemically Produced Ketyl of Perfluorobenzophenone: Electron Spin Resonance Studies of Solvent Effects.
Sargent FP and Bailey MG.
Canadian Journal of Chemistry, 51(19), 3211-3216 (1973)



Global Trade Item Number

SKUGTIN
F8761-5G04061832343099
F8761-1G04061826116838
F8761-25G04061833621028
101893-5G04061831809671