2-(Trifluoromethyl)benzonitrile
Names
[ CAS No. ]:
447-60-9
[ Name ]:
2-(Trifluoromethyl)benzonitrile
[Synonym ]:
NCR BXFFF
ortho-trifluoromethylbenzonitrile
trifluoromethylbenzonitrile
o-Trifluoromethylbenzonitrile
2-(Trifluoromethyl)benzonitrile
o-(Trifluoromethyl)benzonitrile
Benzonitrile, 2-(trifluoromethyl)-
2-Cyanobenzotrifluoride
EINECS 207-184-3
α,α,α-trifluoro-o-tolunitrile
a,a,a-trifluoro-o-tolunitrile
bistrifluoromethylbenzonitrile
MFCD00001791
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ Boiling Point ]:
205.0±35.0 °C at 760 mmHg
[ Melting Point ]:
7.5 °C(lit.)
[ Molecular Formula ]:
C8H4F3N
[ Molecular Weight ]:
171.119
[ Flash Point ]:
90.0±0.0 °C
[ Exact Mass ]:
171.029587
[ PSA ]:
23.79000
[ LogP ]:
2.63
[ Vapour Pressure ]:
0.3±0.4 mmHg at 25°C
[ Index of Refraction ]:
1.461
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H302
[ 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 ]:
R22
[ Safety Phrases ]:
S61
[ RIDADR ]:
UN 3276 6.1/PG 3
[ WGK Germany ]:
2
[ Packaging Group ]:
III
[ Hazard Class ]:
6.1
[ HS Code ]:
2926909090
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
Int. J. Oncol. 46(4) , 1560-72, (2015)
Resistance of prostate cancer to castration is currently an unavoidable problem. The major mechanisms underlying such resistance are androgen receptor (AR) overexpression, androgen-independent activat...
An efficient method for the conversion of aromatic and aliphatic nitriles to the corresponding N-tert-butyl amides: a modified Ritter reaction. Reddy KL.Tetrahedron Lett. 44(7) , 1453-55, (2003)
A convenient and efficient protocol for the synthesis of symmetrical N,N'-alkylidine bisamides by sulfamic acid under solvent-free conditions. Selvam NP, et al.
Can. J. Chem. 86(1) , 32-38, (2008)