| Weight | 136.15 g/mol |
|---|---|
| Formula | C8H8O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-Hydroxy-5-methylbenzaldehyde (613-84-3)
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- New organotin(IV) complexes with N(4)-methylthiosemicarbazone derivatives prepared from 2,3-dihydroxybenzaldehyde and 2-hydroxy-5-methylbenzaldehyde: synthesis, characterization, and cytotoxic activity (Journal of Coordination Chemistry, 2015)
- Anodic pyridination of 2-hydroxy-3-methoxy-5-methylbenzaldehyde and its Schiff's base derivatives (Journal of The Chemical Society-perkin Transactions 1, 1980)
- Anodic acetoxylation of 2-hydroxy-3-methoxy-5-methylbenzaldehyde and its Schiff bases. (Chemical & Pharmaceutical Bulletin, 1980)
- Regiospecific anodic pyridination of 2-hydroxy-3-methoxy-5-methylbenzaldehyde Schiff bases (Journal of The Chemical Society, Chemical Communications, 1978)
- ChemInform Abstract: REGIOSPECIFIC ANODIC PYRIDINATION OF 2-HYDROXY-3-METHOXY-5-METHYLBENZALDEHYDE SCHIFF BASES (ChemInform, 1978)
- ChemInform Abstract: ANODIC PYRIDINATION OF 2-HYDROXY-3-METHOXY-5-METHYLBENZALDEHYDE AND ITS SCHIFF BASE DERIVATIVES (ChemInform, 1980)
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SMILESCC1=CC(=C(C=C1)O)C=O
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InChIKeyILEIUTCVWLYZOM-UHFFFAOYSA-N
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