| Weight | 132.162 g/mol |
|---|---|
| Formula | C9H8O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
cinnamaldehyde
cinnamic aldehyde · trans-3-phenylprop-2-enaldehyde · beta-phenylacrolein
14371-10-9, 104-55-2, 57194-69-1
Score:
#641 in Biology
,
#684 in Chemistry
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- INHIBITION OF GROWTH AND AFLATOXIN PRODUCTION BY CINNAMON AND CLOVE OILS. CINNAMIC ALDEHYDE AND EUGENOL (Journal of Food Science, 1977)
- Changes in membrane fatty acids composition of microbial cells induced by addiction of thymol, carvacrol, limonene, cinnamaldehyde, and eugenol in the growing media. (Journal of Agricultural and Food Chemistry, 2006)
- Cinnamaldehyde--a potential antidiabetic agent. (Phytomedicine, 2007)
- Mechanisms of bactericidal action of cinnamaldehyde against Listeria monocytogenes and of Eugenol against L. monocytogenes and Lactobacillus sakei (Applied and Environmental Microbiology, 2004)
- Pd nanoparticles introduced inside multi-walled carbon nanotubes for selective hydrogenation of cinnamaldehyde into hydrocinnamaldehyde (Applied Catalysis A-general, 2005)
- TRPA1 and TRPM8 activation in humans: effects of cinnamaldehyde and menthol. (Neuroreport, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - cinnamic aldehyde
- trans-3-phenylprop-2-enaldehyde
- beta-phenylacrolein
- supercinnamaldehyde
- 3-phenylprop-2-enaldehyde
- cinnamic aldehyde, (E)-isomer
-
SMILESC1=CC=C(C=C1)C=CC=O
-
InChIKeyKJPRLNWUNMBNBZ-UHFFFAOYSA-N
- Pubchem - cinnamaldehyde
- Wikipedia - cinnamaldehyde
Cinnamaldehyde is an organic compound with the formula C6H5CH=CHCHO. Occurring naturally as predominantly the trans (E) isomer, it gives cinnamon its flavor and odor. It is a flavonoid that is naturally synthesized by the shikimate pathway.
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
Similar Compounds
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cinnamaldehyde
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