| Weight | 148.205 g/mol |
|---|---|
| Formula | C10H12O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,4,6-TRIMETHYLBENZALDEHYDE (487-68-3)
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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)
- CLIII.The nitration of 2 : 4 : 6-trimethylbenzaldehyde (Journal of The Chemical Society (resumed), 1931)
- 3, 6-Dinitro-2, 4, 5-trimethylbenzaldehyde (1973)
- Synthesis of 2,4,6-Trimethylbenzaldehyde (Fine Chemical Intermediates, 2005)
- A New Method for Preparing 2,4,6-Trimethylbenzaldehyde (Chinese Journal of Synthetic Chemistry, 2007)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC(=C(C(=C1)C)C=O)C
-
InChIKeyHIKRJHFHGKZKRI-UHFFFAOYSA-N
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2,4,6-TRIMETHYLBENZALDEHYDE
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