144614
4-Chlorocinnamonitrile, mixture of cis and trans
98%
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Assay
98%
form
solid
mp
55-70 °C (lit.)
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. It was used to compare the radical and homocopolymerization ability of geometrical isomers of cinnamonitriles.
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Radical homo-and copolymerization of ring-substituted trans-and cis-cinnamonitriles.
Makromol. Chem., Rapid Commun., 14(10), 649-655 (1993)
Diethoxymethylphosphonites and phosphinates. Intermediates for thesynthesis of a, ?-and X aminoalkylphosphonous acids.
Tetrahedron, 45(12), 3787-3808 (1989)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service