| Weight | 146.145 g/mol |
|---|---|
| Formula | C9H6O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
coumarin (91-64-5)
1,2-benzopyrone · 5,6-benzo-alpha-pyrone
Score:
#263 in Biochemistry
,
#383 in Physics
,
#1130 in Chemistry
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- Low-molecular-weight heparin versus a coumarin for the prevention of recurrent venous thromboembolism in patients with cancer. (The New England Journal of Medicine, 2003)
- Subpicosecond Measurements of Polar Solvation Dynamics: Coumarin 153 Revisited (The Journal of Physical Chemistry, 1995)
- Photocontrolled reversible release of guest molecules from coumarin-modified mesoporous silica (Nature, 2003)
- Molecular Design of Coumarin Dyes for Efficient Dye-Sensitized Solar Cells (Journal of Physical Chemistry B, 2003)
- Picosecond solvation dynamics of coumarin 153: The importance of molecular aspects of solvation (Journal of Chemical Physics, 1987)
- Solvent effects on emission yield and lifetime for coumarin laser dyes. Requirements for a rotatory decay mechanism (The Journal of Physical Chemistry, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H402: Harmful to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 3 - 1,2-benzopyrone
- 5,6-benzo-alpha-pyrone
-
SMILESC1=CC=C2C(=C1)C=CC(=O)O2
-
InChIKeyZYGHJZDHTFUPRJ-UHFFFAOYSA-N
- Pubchem - coumarin
- Wikipedia - coumarin
Coumarin (; 2H-chromen-2-one) is a fragrant organic chemical compound in the benzopyrone chemical class, although it may also be seen as a subclass of lactones. It is a natural substance found in many plants, and a colorless crystalline substance in its standard state. The name comes from a French term for the tonka bean, coumarou, one of the sources from which coumarin was first isolated as a natural product in 1820.
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coumarin
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