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232963

Sigma-Aldrich

4-(Trifluoromethyl)phenylacetonitrile

98%

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About This Item

Linear Formula:
CF3C6H4CH2CN
CAS Number:
Molecular Weight:
185.15
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

bp

131-132 °C/20 mmHg (lit.)

mp

47-49 °C (lit.)

SMILES string

FC(F)(F)c1ccc(CC#N)cc1

InChI

1S/C9H6F3N/c10-9(11,12)8-3-1-7(2-4-8)5-6-13/h1-4H,5H2

InChI key

QNKOCFJZJWOXDE-UHFFFAOYSA-N

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

Pictograms

Exclamation mark

Signal Word

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Deleterious substance

JAN Code

232963-BULK:
232963-5G:4548173121369
232963-1G:4548173121352
232963-VAR:


Certificates of Analysis (COA)

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A Steady Operation of n-Type Organic Thin-Film Transistors with Cyano-Substituted Distyrylbenzene Derivative.
Nagamatsu S, et al.
Applied Physics Express, 2(10), 101502-101502 (2009)
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
Synthesis and FET characteristics of phenylene-vinylene and anthracene-vinylene compounds containing cyano groups.
Shoji K, et al.
Journal of Materials Chemistry, 20(31), 6472-6478 (2010)

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