| Weight | 148.205 g/mol |
|---|---|
| Formula | C10H12O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Mesitaldehyde (487-68-3)
2,4,6-trimethylbenzaldehyde
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- The Reaction between Duroquinone and Sodium Malonic Esters. II. The Synthesis and Reactions of 2,5-Dimethoxy-3,4,6-trimethylbenzaldehyde (Journal of the American Chemical Society, 1934)
- Electrochemical reduction of 2,4,6-trimethylbenzoyl chloride and 2,4,6-trimethylbenzaldehyde at carbon and mercury cathodes in acetonitrile (Electrochimica Acta, 1994)
- The Crystal Structure of Mesitaldehyde-Perchloric Acid 2:1 Adduct (Journal of the American Chemical Society, 1965)
- Adducts of Mesitaldehyde and Strong Molecular Acids (Journal of the American Chemical Society, 1965)
- CLIII.The nitration of 2 : 4 : 6-trimethylbenzaldehyde (Journal of The Chemical Society (resumed), 1931)
- Conformational analysis. Part 6. A lanthanide-induced shift nuclear magnetic resonance investigation of steric effects in mesitaldehyde and 2,4,6-trimethylacetophenone (Journal of The Chemical Society-perkin Transactions 1, 1983)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,4,6-trimethylbenzaldehyde
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SMILESCC1=CC(=C(C(=C1)C)C=O)C
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InChIKeyHIKRJHFHGKZKRI-UHFFFAOYSA-N
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Similar Compounds
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3-Methylbenzoyl chloride
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Mesitaldehyde
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