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139416

4-Fluorobenzonitrile

99%

Synonym(s):

1-Cyano-4-fluorobenzene, 4-Cyanofluorobenzene, 4-Fluorobenzonitrile, 4-Fluorocyanobenzene, Para-fluorobenzonitrile, p-Cyanofluorobenzene, p-Fluorobenzonitrile, p-Fluorophenyl cyanide

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5 g

Available to ship TODAYfromMILWAUKEE

$57.60
25 g

Available to ship TODAYfromMILWAUKEE

$65.30

About This Item

Linear Formula:
FC6H4CN
CAS Number:
1194-02-1
Molecular Weight:
121.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848410
EC Number:
214-784-9
Beilstein/REAXYS Number:
2041517
MDL number:
MFCD00001812
Assay:
99%
Form:
solid

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Quality Level

200

assay

99%

form

solid

bp

188 °C/750 mmHg (lit.)

mp

32-34 °C (lit.)

functional group

fluoro, nitrile

SMILES string

Fc1ccc(cc1)C#N

InChI

1S/C7H4FN/c8-7-3-1-6(5-9)2-4-7/h1-4H

InChI key

AEKVBBNGWBBYLL-UHFFFAOYSA-N

General description

4-Fluorobenzonitrile undergoes metal-mediated coupling to yield eight-membered thorium(IV) tetraazamacrocycle[1]. It undergoes condensation with diphenylamine to yield monomer 4-cyanotriphenylamine.

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This Item
196649144061124826
4-Fluorobenzonitrile 99%

Sigma-Aldrich

139416

4-Fluorobenzonitrile

2-Fluorobenzonitrile 98%

Sigma-Aldrich

196649

2-Fluorobenzonitrile

4-(Bromomethyl)benzonitrile 99%

Sigma-Aldrich

144061

4-(Bromomethyl)benzonitrile

4-Cyanobenzoyl chloride 98%

Sigma-Aldrich

124826

4-Cyanobenzoyl chloride

assay

99%

assay

98%

assay

99%

assay

98%

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

100

mp

32-34 °C (lit.)

mp

-

mp

115-117 °C (lit.)

mp

68-70 °C (lit.)

bp

188 °C/750 mmHg (lit.)

bp

90 °C/21 mmHg (lit.)

bp

-

bp

-

form

solid

form

liquid

form

solid

form

solid

functional group

fluoro, nitrile

functional group

fluoro, nitrile

functional group

bromo, nitrile

functional group

acyl chloride, nitrile

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Sol. 1

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 3

flash_point_f

149.0 °F - closed cup

flash_point_c

65 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB6497
SDBB5510
SDBB1597
STBL0552
STBK9276

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Poly (triphenylamine) s derived from oxidative coupling reaction: Substituent effects on the polymerization, electrochemical, and electro-optical properties.
Lin H-Y and Liou G-S.
Journal of Polymer Science Part A: Polymer Chemistry, 47(1), 285-294 (2009)
Eric J Schelter et al.
Chemical communications (Cambridge, England), (10)(10), 1029-1031 (2007-02-28)
An eight-membered thorium(IV) tetraazamacrocycle is produced by the sequential, metal-mediated coupling of four equivalents of 4-fluorobenzonitrile; its formation is consistent with the involvement of an imido intermediate, generated from a thorium ketimide complex.
Oriol Planas et al.
Science (New York, N.Y.), 367(6475), 313-317 (2020-01-18)
Bismuth catalysis has traditionally relied on the Lewis acidic properties of the element in a fixed oxidation state. In this paper, we report a series of bismuth complexes that can undergo oxidative addition, reductive elimination, and transmetallation in a manner
View All Related Papers

Global Trade Item Number

SKUGTIN
139416-25G04061838732842
139416-5G04061838732859

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