| Weight | 120.151 g/mol |
|---|---|
| Formula | C8H8O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-Methylbenzaldehyde (529-20-4)
o-tolualdehyde
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- The Synthesis of -Amino-o-tolualdehyde Diethylacetal and its Attempted Conversion to Pseudoisoindole (Journal of the American Chemical Society, 1956)
- Gas phase hydrogenation/hydrogenolysis of benzaldehyde and o-tolualdehyde over Ni/SiO2 (Journal of Molecular Catalysis A-chemical, 1997)
- A New Synthesis of Atranol (2,6-Dihydroxy-4-methylbenzaldehyde) and the Corresponding Cinnamic Acid (Journal of the American Chemical Society, 1948)
- Methyleneketenes and methylenecarbenes. II. A new phenolic ring synthesis: 2-Naphthol from o-tolualdehyde (Australian Journal of Chemistry, 1974)
- Condensation of a supersaturated vapor. V. The nucleating effects of ultraviolet light on vapors containing very low concentrations of otolualdehyde (Journal of Chemical Physics, 1981)
- A three-step synthesis of an enantiomerically pure halostachine analogic starting from 6 (o-tolualdehyde)-chromium-tricarbonyl. (Tetrahedron-asymmetry, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - o-tolualdehyde
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SMILESCC1=CC=CC=C1C=O
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InChIKeyBTFQKIATRPGRBS-UHFFFAOYSA-N
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Similar Compounds
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2-Methylbenzaldehyde
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