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Merck
CN

115622

4-Chlorobenzonitrile

99%

Synonym(s):

1-Chloro-4-benzonitrile, 1-Chloro-4-cyanobenzene, 4-Cyanophenyl chloride, p-Chlorobenzonitrile

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About This Item

Linear Formula:
ClC6H4CN
CAS Number:
Molecular Weight:
137.57
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39050680
UNSPSC Code:
12352100
EC Number:
210-765-4
MDL number:
Beilstein/REAXYS Number:
1072122
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Product Name

4-Chlorobenzonitrile, 99%

InChI

1S/C7H4ClN/c8-7-3-1-6(5-9)2-4-7/h1-4H

InChI key

GJNGXPDXRVXSEH-UHFFFAOYSA-N

SMILES string

Clc1ccc(cc1)C#N

assay

99%

form

solid

bp

223 °C (lit.)

mp

90-93 °C (lit.)

functional group

chloro
nitrile

Quality Level

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Application

4-Chlorobenzonitrile has been used in the preparation of amides.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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 2

flash_point_f

226.4 °F

flash_point_c

108 °C

ppe

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


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Ondrej Kaplan et al.
Applied microbiology and biotechnology, 73(3), 567-575 (2006-10-25)
Aspergillus niger K10 cultivated on 2-cyanopyridine produced high levels of an intracellular nitrilase, which was partially purified (18.6-fold) with a 24% yield. The N-terminal amino acid sequence of the enzyme was highly homologous with that of a putative nitrilase from
Luca Quattrini et al.
Scientific reports, 9(1), 9943-9943 (2019-07-11)
Melanoma is the most serious form of skin cancer but its medication is still far from being safe and thoroughly effective. The search of novel therapeutic approaches represents therefore a health emergency to push through eagerly. In this study, we

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