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Key Documents

144614

Sigma-Aldrich

4-Chlorocinnamonitrile, mixture of cis and trans

98%

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About This Item

Linear Formula:
ClC6H4CH=CHCN
CAS Number:
Molecular Weight:
163.60
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

mp

55-70 °C (lit.)

functional group

chloro
nitrile

SMILES string

Clc1ccc(\C=C\C#N)cc1

InChI

1S/C9H6ClN/c10-9-5-3-8(4-6-9)2-1-7-11/h1-6H/b2-1+

InChI key

PPCNBCKABHGVMX-OWOJBTEDSA-N

Application

4-Chlorocinnamonitrile was used in the synthesis of ethyl-1-(4-chlorophenyl)-2-cyanoethyl(diethoxymethyl)phosphinate[1]. It was used to compare the radical and homocopolymerization ability of geometrical isomers of cinnamonitriles[2].

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Classifications

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

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Diethoxymethylphosphonites and phosphinates. Intermediates for thesynthesis of a, ?-and X aminoalkylphosphonous acids.
Dingwalla JG, et al.
Tetrahedron, 45(12), 3787-3808 (1989)
Radical homo-and copolymerization of ring-substituted trans-and cis-cinnamonitriles.
Tanaka H, et al.
Makromol. Chem., Rapid Commun., 14(10), 649-655 (1993)

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