| Weight | 174.155 g/mol |
|---|---|
| Formula | C10H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Chromone-3-carboxaldehyde (17422-74-1)
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- A facile synthesis of chromone-3-carboxaldehyde, chromone-3-carboxylic acid and 3-hydroxymethylchromone (Tetrahedron Letters, 1973)
- Novel transformation of chromone-3-carboxaldehyde to an o-hydroxybenzophenone (Journal of Organic Chemistry, 1976)
- Synthesis and characterization of new metal complexes of thiosemicarbazone derived from 4-phenyl-3-thiosemicarbazide and chromone-3-carboxaldehyde (Transition Metal Chemistry, 1988)
- Condensation of chromone-3-carboxaldehyde with phenylacetic acids: An efficient synthesis of (E)-3-styrylchromones (Synlett, 2004)
- Studies in chromone derivatives: cycloaddition reactions of 4-oxo 4h-1-benzopyran-3-carboxaldehyde imines with benzonitrile oxide and nitrilimine of 4-oxo-4h-1-benzopyran-3-carboxaldehyde with alkenes (Tetrahedron, 1988)
- Synthesis and Spectroscopic Studies of New Metal Complexes of Thiosemicarbazones Derived from 4-Ethyl-3-Thiosemicarbazide and Biacetylmonoxime. Chromone-3-Carboxaldehyde or Isatin (Synthesis and Reactivity in Inorganic and Metal-organic Chemistry, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C(=O)C(=CO2)C=O
-
InChIKeyFSMYWBQIMDSGQP-UHFFFAOYSA-N
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