| Weight | 134.134 g/mol |
|---|---|
| Formula | C8H6O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Coumaranone (553-86-6)
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- Flash-thermolysis of methylenephtalide and 3-methylene-2-coumaranone (Tetrahedron Letters, 1981)
- Aurone biosynthesisII. : Formation of 4,6-dihydroxy-2-(-hydroxybenzyl)coumaranone from 2,4,4-trihydroxychalcone by cell-free extracts of soybean (Phytochemistry, 1967)
- The photodegradation of 2,3-benzofuran and its intermediates, 2-coumaranone and salicylaldehyde, in TiO2 aqueous suspensions (Journal of Photochemistry and Photobiology A-chemistry, 1995)
- Hypervalent Iodine Oxidation of 1-Trimethylsilyloxy, 1-(2-Trimethylsilyloxyphenyl)Ethene. Synthesis of 3-Coumaranone and 2,2-Dihydroxyacetophenone (Synthetic Communications, 1986)
- Products obtained from the reaction of molecular oxygen with the sodium salts of 3-phenyloxindoles and 3-phenyl-2-coumaranone (Journal of Organic Chemistry, 1968)
- Remote induction of the condensation of p-nitrobenzaldehyde on the methylene group of 5-hydroxy-2-coumaranone (Heterocycles, 1988)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C2=CC=CC=C2OC1=O
-
InChIKeyACZGCWSMSTYWDQ-UHFFFAOYSA-N
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2-Coumaranone
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