232963
4-(Trifluoromethyl)phenylacetonitrile
98%
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About This Item
Linear Formula:
CF3C6H4CH2CN
CAS Number:
Molecular Weight:
185.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
219-052-2
MDL number:
Assay:
98%
Form:
solid
InChI key
QNKOCFJZJWOXDE-UHFFFAOYSA-N
InChI
1S/C9H6F3N/c10-9(11,12)8-3-1-7(2-4-8)5-6-13/h1-4H,5H2
SMILES string
FC(F)(F)c1ccc(CC#N)cc1
assay
98%
form
solid
bp
131-132 °C/20 mmHg (lit.)
mp
47-49 °C (lit.)
functional group
fluoro, nitrile
Quality Level
Related Categories
Application
4-(Trifluoromethyl)phenylacetonitrile was used in the preparation of:
- 1,4-bis[2-cyano-2-(4-(trifluoromethyl)phenyl)vinyl]benzene
- cyano-substituted distyrylbenzene derivative, novel n-type organic semiconductor
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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A Steady Operation of n-Type Organic Thin-Film Transistors with Cyano-Substituted Distyrylbenzene Derivative.
Nagamatsu S, et al.
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Shoji K, et al.
Journal of Materials Chemistry, 20(31), 6472-6478 (2010)
Immacolata Serra et al.
Marine biotechnology (New York, N.Y.), 21(2), 229-239 (2019-01-27)
A screening among marine yeasts was carried out for nitrile hydrolyzing activity. Meyerozyma guilliermondii LM2 (UBOCC-A-214008) was able to efficiently grow on benzonitrile and cyclohexanecarbonitrile (CECN) as sole nitrogen sources. A two-step one-pot method for obtaining cells of M. guilliermondii
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