Weight | 166.176 g/mol |
---|---|
Formula | C9H10O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
2,4-Dimethoxybenzaldehyde (613-45-6)
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- Synthesis and Characterization of Two Diimine Schiff Bases Derived from 2,4-Dimethoxybenzaldehyde: The Crystal Structure of N,N'-Bis(2,4-dimethoxy- benzylidene)-1,2-diaminoethane (Acta Chimica Slovenica, 2010)
- A New Synthesis of 3-Fluoroveratrole and 2-Fluoro-3, 4-Dimethoxybenzaldehyde (Synthetic Communications, 1985)
- Highly Selective and Sensitive Triiodide PVC-Membrane Electrode Based on a New Charge-Transfer Complex of Bis(2,4-Dimethoxybenzaldehyde)butane-2,3-Dihydrazone with Iodine (Journal of The Chinese Chemical Society, 2006)
- Selective Preparation of 4-(Bromo or Iodo)-2,5-dimethoxybenzonitrile and 2-(Bromo or Iodo)-3,6-dimethoxybenzonitrile from 2,5-Dimethoxybenzaldehyde (Synthetic Communications, 1998)
- [An attempt to synthesize dl-cularine by the decomposition of 2-(1,2,3,4-tetrahydro-7-methoxy-2-methyl-8-isoquinolinoxy)-4,5-dimethoxybenzaldehyde p-toluenesulphonylhydrazone under alkaline condition]. (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1970)
- Mechanism of the cross Cannizzaro reaction of 2, 4-dimethoxybenzaldehyde with formaldehyde in aqueous KOH solutions (Russian Chemical Bulletin, 1975)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC(=C(C=C1)C=O)OC
-
InChIKeyLWRSYTXEQUUTKW-UHFFFAOYSA-N
- Pubchem - 2,4-Dimethoxybenzaldehyde
- Wikipedia - 2,4-Dimethoxybenzaldehyde
2,4-Dimethoxybenzaldehyde (DMBA) is a reagent used to specifically quantify phlorotannins. This product reacts specifically with 1,3-and 1,3,5-substituted phenols (e.g., phlorotannins) to form a colored product.
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