perfluoronitrobenzene
Suppliers
Names
[ CAS No. ]:
880-78-4
[ Name ]:
perfluoronitrobenzene
[Synonym ]:
1,2,3,4,5-Pentafluoro-6-nitrobenzene
nitropentafluorobenzene
Pentafluoronitrobenzene
perfluoronitrobenzene
Benzene, 1,2,3,4,5-pentafluoro-6-nitro-
EINECS 212-915-4
Benzene, pentafluoronitro-
MFCD00007049
Chemical & Physical Properties
[ Density]:
1.7±0.1 g/cm3
[ Boiling Point ]:
159.5±0.0 °C at 760 mmHg
[ Melting Point ]:
-22.65°C
[ Molecular Formula ]:
C6F5NO2
[ Molecular Weight ]:
213.062
[ Flash Point ]:
90.6±0.0 °C
[ Exact Mass ]:
212.984924
[ PSA ]:
45.82000
[ LogP ]:
1.11
[ Vapour Pressure ]:
3.2±0.2 mmHg at 25°C
[ Index of Refraction ]:
1.448
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36/37/39
[ WGK Germany ]:
3
[ HS Code ]:
2904909090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2904909090
[ Summary ]:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
Articles
J. Org. Chem. 65(16) , 4949-53, (2000)
p-Azidotetrafluoroaniline (1) was synthesized in 65-73% yield by two different methods employing a stable carbamate intermediate. The first method trapped the intermediate isocyanate generated via a m...
Phys. Chem. Chem. Phys. 10(11) , 1523-31, (2008)
Electron attachment to pentafluorobenzonitrile (C(6)F(5)CN) and pentafluoronitrobenzene (C(6)F(5)NO(2)) is studied in the energy range 0-16 eV by means of a crossed electron-molecular beam experiment ...
Voltammetry under high mass transport conditions. The application of the high speed channel electrode to the reduction of pentafluoronitrobenzene. Coles BA, et al.J. Electroanal. Chem. 411(1) , 121-27, (1996)