| Weight | 152.624 g/mol |
|---|---|
| Formula | C9H9Cl |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Cinnamyl chloride (2687-12-9, 21087-29-6)
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- Sigma-Aldrich - Cinnamyl chloride25.90 - 103.50 USD
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- TCI - Cinnamyl chloride61.00 USD
- Reductive generation of active zero-valent in SnCl2Al system and its use for highly diastereoselective reaction of cinnamyl chloride and aldehydes. (Tetrahedron Letters, 1986)
- FACTORS DETERMINING THE COURSE AND MECHANISM OF GRIGNARD REACTIONS. XVIII. THE EFFECT OF METALLIC HALIDES ON THE REACTIONS OF GRIGNARD REAGENTS WITH 1-PHENYL-3-CHLOROPROPANE, CINNAMYL CHLORIDE, AND PHENYLETHYNYL BROMIDE (Journal of Organic Chemistry, 1945)
- Lithiation of Cinnamyl Chloride: Stereoselective Synthesis of Propargylic Oxiranes and Aziridines (European Journal of Organic Chemistry, 2000)
- Allylic Chlorides. XII. Preparation and Properties of cis- and trans-Cinnamyl Chloride (Journal of the American Chemical Society, 1950)
- Highly diastereoselective reactions of (E)-cinnamyl chloride with aldehydes mediated by tin and aluminium (Tetrahedron Letters, 1985)
- Highly Selective Epoxidation of -Pinene and Cinnamyl Chloride with Dry Air over Nanosized Metal Oxides (Catalysis Letters, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C=CCCl
-
InChIKeyIWTYTFSSTWXZFU-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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Cinnamyl chloride
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