2-Fluorobenzonitrile
Names
[ CAS No. ]:
394-47-8
[ Name ]:
2-Fluorobenzonitrile
[Synonym ]:
Benzonitrile, 2-fluoro-
NCR BF
Benzonitrile,o-fluoro
o-Fluorobenzonitrile
EINECS 206-897-7
2-Fluorobenzenenitrile
1-CYANO-2-FLUOROBENZENE
o-Cyanofluorobenzene
Benzonitrile,2-fluoro
2-Fluorobenzonitrile
2-fluoro-benzonitrile
2-Fluorobenzenecarbonitrile
MFCD00001773
2-FLUOROBENZONITRIL
2-Cyanofluorobenzene
2-fluorocyanobenzene
Letrozole Impurity 9
Chemical & Physical Properties
[ Density]:
1.2±0.1 g/cm3
[ Boiling Point ]:
193.6±0.0 °C at 760 mmHg
[ Melting Point ]:
35 - 37ºC
[ Molecular Formula ]:
C7H4FN
[ Molecular Weight ]:
121.112
[ Flash Point ]:
73.9±0.0 °C
[ Exact Mass ]:
121.032776
[ PSA ]:
23.79000
[ LogP ]:
1.51
[ Vapour Pressure ]:
0.5±0.3 mmHg at 25°C
[ Index of Refraction ]:
1.511
[ Storage condition ]:
Refrigerator
MSDS
Safety Information
[ Symbol ]:
GHS05, GHS07
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H302-H315-H318-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-S39-S36/37/39
[ RIDADR ]:
3276
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ HS Code ]:
29269095
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2926909090
[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
Articles
Analyst 140 , 8177-85, (2015)
The rising importance of organohalogens in environmental, pharmaceutical, and biological applications has drawn attention to analysis of these compounds in recent years. Elemental mass spectrometry (M...
Studies on the synthetic compatibility of aryloxime linkers in the solid-phase synthesis of 3-aminobenzisoxazoles.J. Org. Chem. 65(10) , 2924-32, (2000)
Further exploration of the scope of our solid-phase method for the synthesis of 3-aminobenzisoxazoles (using the Kaiser oxime resin 1) is described. The effects of base, leaving group, and solvent on ...
Aminoborohydrides. 12. Novel tandem S(N)Ar amination-reduction reactions of 2-halobenzonitriles with lithium N,N-dialkylaminoborohydrides.J. Org. Chem. 66(6) , 1999-2004, (2001)
A novel tandem amination-reduction reaction has been developed in which 2-(N,N-dialkylamino)benzylamines are generated from 2-halobenzonitriles and lithium N,N-dialkylaminoborohydride (LAB) reagents. ...