Coumarin
| Names | |
|---|---|
| IUPAC name 2H-Chromen-2-one | |
| Preferred IUPAC name 2H-1-Benzopyran-2-one | |
| Other names 1-Benzopyran-2-one | |
| Identifiers | |
| 3D model (JSmol) | |
| 383644 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.001.897 | 
| EC Number | 
 | 
| 165222 | |
| KEGG | |
| PubChem CID | |
| RTECS number | 
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| UNII | |
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C9H6O2 | |
| Molar mass | 146.145 g·mol−1 | 
| Appearance | colorless to white crystals | 
| Odor | pleasant, like vanilla beans | 
| Density | 0.935 g/cm3 (20 °C (68 °F)) | 
| Melting point | 71 °C (160 °F; 344 K) | 
| Boiling point | 301.71 °C (575.08 °F; 574.86 K) | 
| 0.17 g / 100 mL | |
| Solubility | very soluble in ether, diethyl ether, chloroform, oil, pyridine soluble in ethanol | 
| log P | 1.39 | 
| Vapor pressure | 1.3 hPa (106 °C (223 °F)) | 
| −82.5×10−6 cm3/mol | |
| Structure | |
| orthorhombic | |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H302, H317, H373 | |
| P260, P261, P264, P270, P272, P280, P301+P312, P302+P352, P314, P321, P330, P333+P313, P363, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | 150 °C (302 °F; 423 K) | 
| Lethal dose or concentration (LD, LC): | |
| LD50 (median dose) | 293 mg/kg (rat, oral) | 
| Safety data sheet (SDS) | Sigma-Aldrich | 
| Related compounds | |
| Related compounds | Chromone; 2-Cumaranone | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Coumarin (/ˈkuːmərɪn/) or 2H-chromen-2-one is an aromatic organic chemical compound with formula C9H6O2. Its molecule can be described as a benzene molecule with two adjacent hydrogen atoms replaced by an unsaturated lactone ring −(CH)=(CH)−(C=O)−O−, forming a second six-membered heterocycle that shares two carbons with the benzene ring. It belongs to the benzopyrone chemical class and is considered a lactone.
Coumarin is a colorless crystalline solid with a sweet odor resembling the scent of vanilla and a bitter taste. It is found in many plants, where it may serve as a chemical defense against predators. While coumarin is not an anticoagulant, its 3-alkyl-4-hydroxy derivatives, such as the fungal metabolite dicoumarol, inhibit synthesis of vitamin K, a key component in blood clotting. A related compound, the prescription drug anticoagulant warfarin, is used to inhibit formation of blood clots, deep vein thrombosis, and pulmonary embolism.