| Weight | 168.192 g/mol |
|---|---|
| Formula | C9H12O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
1,2,4-Trimethoxybenzene (135-77-3)
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- Ozonolysis of lignin models in aqueous solution: anisole, 1,2-dimethoxybenzene, 1,4-dimethoxybenzene, and 1,3,5-trimethoxybenzene. (Environmental Science & Technology, 2009)
- Trifluoromethanesulfonic Acid Catalyzed FriedelCrafts Alkylations of 1,2,4-Trimethoxybenzene with Aldehydes or Benzylic Alcohols (Organic Letters, 2013)
- Photoinitiated radical polymerization using charge transfer complex of Nethoxypcyanopyridinium salt and 1,2,4trimethoxybenzene (Polymer International, 1998)
- Polycyclic Aromatic Nitrogen Heterocycles. Part IV: Effect of Solvent Polarity, Solvent Acidity, Nitromethane and 1,2,4-Trimethoxybenzene on the Fluorescence Emission Behavior of Select Monoaza- and Diazaarenes (Applied Spectroscopy, 1992)
- Metalation reactions. XVI. Polylithiation of 1,3,5- and 1,2,4-trimethoxybenzene (Tetrahedron, 1991)
- N-Halogeno compounds. Part 20. Vicarious electrophilic fluorodemethylation of 1,3,5-trimethoxybenzene and 2,4,6-trimethoxytoluene with 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor reagent F-TEDA-BF4) (Journal of Fluorine Chemistry, 1999)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCOC1=CC(=C(C=C1)OC)OC
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InChIKeyAGIQIOSHSMJYJP-UHFFFAOYSA-N
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1,2,4-Trimethoxybenzene
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