| Weight | 277.106 g/mol |
|---|---|
| Formula | C14H6Cl2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
1,8-Dichloroanthraquinone (82-43-9)
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- The excited state dynamics of triplet 1,8dichloroanthraquinone in solutions at room temperature (Journal of Chemical Physics, 1986)
- Observation of a new absorption due to a precursor of the lowest triplet state of 1,8-dichloroanthraquinone (Chemical Physics Letters, 1984)
- Primary photoreduction of 1,8-dichloroanthraquinone by triethylamine studied by laser spectroscopy (Journal of Photochemistry, 1985)
- Syntheses and reactions of phosphates from dibromoanthrone. Anthraquinone anil, and 1,8-dichloroanthraquinone (Journal of Organic Chemistry, 1970)
- Formation and decay of an excited singlet charge-transfer complex ( or a singlet ion pair) produced by excitation of a ground-state complex of 1,8-dichloroanthraquinone with 2,5-dimethylhexa-2,4-diene at room temperature (Journal of Photochemistry and Photobiology A-chemistry, 1993)
- Unusual monosubstitution-monodechlorination product in the reaction of 1,8-dichloroanthraquinone with (S)-()-2-(tetrahydropyranyloxy)-1-propanol (Tetrahedron, 1997)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C(=C1)Cl)C(=O)C3=C(C2=O)C=CC=C3Cl
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InChIKeyVBQNYYXVDQUKIU-UHFFFAOYSA-N
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