| Weight | 180.59 g/mol |
|---|---|
| Formula | C9H5ClO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
6-Chlorocoumarin (2051-59-4)
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- photocyclization of 2,6-dichlorocinnamic acid derivatives to 5-chlorocoumarin (Journal of Organic Chemistry, 1983)
- An improved synthesis of 4-chlorocoumarin-3-sulfonyl chloride and its reactions with different bidentate nucleophiles to give pyrido[1, 2:2,3]- and thiazino[3,2:2,3]-1,2,4-thiadiazino[6,5-c] benzopyran-6-one 7,7-dioxides (Molecules, 2007)
- Photocyclisation of 2,6-dichlorocinnamates to 5-chlorocoumarin (Journal of The Chemical Society, Chemical Communications, 1976)
- [STUDIES ON THE COUMARIN DERIVATIVES OF MEDICINAL PURPOSES. XV. SYNTHESIS OF 6-CHLOROCOUMARIN-36C1 AND ITS DISTRIBUTION IN VIVO]. (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1963)
- COUMARIN DERIVATIVES FOR MEDICINAL PURPOSES. XV. SYNTHESIS OF 6- CHLOROCOUMARIN-Cl$sup 36$ AND ITS DISTRIBUTION IN VIVO (1963)
- Substitution of a nitro group by formyl or a chlorine atom in 3,6-dinitro-4-chlorocoumarin under vilsmeier-haack conditions (Chemistry of Heterocyclic Compounds, 1988)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=CC(=O)O2)C=C1Cl
-
InChIKeyAMQSYJCKXPUEDR-UHFFFAOYSA-N
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