| Weight | 140.094 g/mol |
|---|---|
| Formula | C6H4O4 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Coumalic acid (500-05-0)
2-oxo-1,2H-pyran-5-carboxylic acid · coumalic acid, sodium salt
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- Aromatics from pyrones: para-substituted alkyl benzoates from alkenes, coumalic acid and methyl coumalate (Green Chemistry, 2011)
- Double Diels-Alder reactions of coumalic acid with 1,3-dienes. (Bulletin of the Chemical Society of Japan, 1979)
- Time-dependent inactivation of chick-embryo prolyl 4-hydroxylase by coumalic acid. Evidence for a syncatalytic mechanism. (Biochemical Journal, 1987)
- Stimulation by Caffeic Acid, Coumalic Acid, and Corilagin of the Germination of Resting Spores of the Clubroot Pathogen Plasmodiophora brassicae (Bioscience, Biotechnology, and Biochemistry, 2003)
- 2-Pyrones. XIII.1The Chemistry of Coumalic Acid and its Derivatives (Journal of the American Chemical Society, 1955)
- Kinetics, reactivity, initial-transition state analysis and thermodynamic parameters of base-catalyzed hydrolysis of coumalic acid in solvents with different polarities (Arabian Journal of Chemistry, 2017)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-oxo-1,2H-pyran-5-carboxylic acid
- coumalic acid, sodium salt
-
SMILESC1=CC(=O)OC=C1C(=O)O
-
InChIKeyORGPJDKNYMVLFL-UHFFFAOYSA-N
- Pubchem - Coumalic acid
- Wikipedia - coumalic acid
Coumalic acid is an organic compound with the molecular formula C6H4O4. Its melting point is around 210 C. In laboratory coumalic acid may be obtained by self-condensation of malic acid in fuming sulfuric acid:
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Coumalic acid
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