| Weight | 166.607 g/mol |
|---|---|
| Formula | C9H7ClO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Cinnamoyl chloride (17082-09-6, 102-92-1)
cinnamoyl chloride, (E)-isomer
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- Sigma-Aldrich - Cinnamoyl chloride23.80 - 105.00 USD
- Fisher Scientific - Search for Cinnamoyl chloride
- TCI - Cinnamoyl chloride20.00 - 94.00 USD
- A Synthetic Strategy for Polyfunctionalized Bicyclo[3.3.1]nonanes Based on a Tandem Three-Component [3 + 2] Cycloaddition of -Cinnamoyl Ketene-S,S-acetals with Oxalyl Chloride (Journal of Organic Chemistry, 2009)
- Cathodic reduction of cinnamoyl chloride (Electrochimica Acta, 1984)
- A remarkable stereocontrol during cobalt(II) chloride catalysed opening of cinnamoyl epoxides with N-substituted anilines (Tetrahedron Letters, 1997)
- On the volumetric determination of small amounts of water by means of cinnamoyl chloride (Mikrochimica Acta, 1937)
- Effect of mesoionic 4-phenyl-5-(cinnamoyl)-1,3,4-thiadiazolium-2-phenylamine chloride derivative salts on the activities of the nitric oxide synthase and arginase of Leishmania amazonensis (Journal of Enzyme Inhibition and Medicinal Chemistry, 2008)
- The Reaction Products from Resorcinol Dimethyl Ether and Cinnamoyl Chloride by the Friedel-Crafts Reaction (Bulletin of the Chemical Society of Japan, 1963)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - cinnamoyl chloride, (E)-isomer
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SMILESC1=CC=C(C=C1)C=CC(=O)Cl
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InChIKeyWOGITNXCNOTRLK-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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Cinnamoyl chloride
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