| Weight | 129.162 g/mol |
|---|---|
| Formula | C9H7N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Cinnamonitrile (1885-38-7, 4360-47-8)
cinnamonitrile, (E)-isomer · cinnamonitrile, (Z)-isomer
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- Electrohydrodimerization Reactions II . Rotating RingDisk Electrode, Voltammetric and Coulometric Studies of Dimethyl Fumarate, Cinnamonitrile, and Fumaronitrile (Journal of The Electrochemical Society, 1972)
- Formation of mercapturic acids from acrylonitrile, crotononitrile, and cinnamonitrile by direct conjugation and via an intermediate oxidation process. (Drug Metabolism and Disposition, 1981)
- A Novel Synthesis of 4-H-Thiopyrans: Unexpected Products of Reaction of Cyanothioacetamide with Cinnamonitrile Derivatives (Heterocycles, 1985)
- Microwaveprompted Reaction of Cinnamonitrile Derivatives with 5,5Dimethyl1,3cyclohexanedione (Chinese Journal of Chemistry, 2010)
- Use of achiral/chiral SFC/MS for the profiling of isomeric cinnamonitrile/hydrocinnamonitrile products in chiral drug synthesis. (Analytical Chemistry, 2006)
- Electrohydrodimerization Reactions III . Rotating RingDisk Electrode, Voltammetric and Coulometric Studies of Mixed Reductive Coupling of Dimethyl Fumarate in the Presence of Cinnamonitrile and Acrylonitrile in Dimethylformamide Solution (Journal of The Electrochemical Society, 1973)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - cinnamonitrile, (E)-isomer
- cinnamonitrile, (Z)-isomer
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SMILESC1=CC=C(C=C1)C=CC#N
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InChIKeyZWKNLRXFUTWSOY-UHFFFAOYSA-N
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Alternate Names
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Synthesis
Reactant
+
CHLOROBENZENE
(Stille)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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Cinnamonitrile
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