2-Fluorobenzonitrile
Suppliers
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...
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 ...
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. ...