| Weight | 180.59 g/mol |
|---|---|
| Formula | C9H5ClO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
3-Chlorocoumarin (92-45-5)
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- Synthesis of 3-arylcoumarins via Suzuki-cross-coupling reactions of 3-chlorocoumarin (Tetrahedron Letters, 2011)
- Preparation and reactions of a 3-chlorocoumarin photodimer. (Journal of Organic Chemistry, 1968)
- Synthesis of [1]Benzopyrano[4,3-b]pyrrol-4(1H)-ones from 4-Chlorocoumarin (Synthesis, 1994)
- 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)
- Phosphorylation and amine-induced dephosphorylation of 4-chlorocoumarin-3-carboxaldehyde and 4-chloro-3-(, -dicyanoethenylidene)coumarin (Phosphorus Sulfur and Silicon and The Related Elements, 2003)
- Unexpected Synthesis of a 5H-chromeno[3,4-c]pyridine Derivative from 4-Chlorocoumarin-3-carbaldehyde and Malononitrile (Journal of Heterocyclic Chemistry, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C=C(C(=O)O2)Cl
-
InChIKeyCKCOPMSBJBNBCQ-UHFFFAOYSA-N
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