| Weight | 146.189 g/mol |
|---|---|
| Formula | C10H10O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
alpha-Methyl cinnamaldehyde (101-39-3, 66051-14-7)
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- Asymmetric synthesis of alpha-amino acids: preparation and alkylation of monocyclic iminolactones derived from alpha-methyl trans-cinnamaldehyde. (Journal of Organic Chemistry, 2008)
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SMILESCC(=CC1=CC=CC=C1)C=O
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InChIKeyVLUMOWNVWOXZAU-UHFFFAOYSA-N
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Synthesis
Reactant
+
CHLOROBENZENE
(Stille)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
Similar Compounds
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