| Weight | 180.206 g/mol |
|---|---|
| Formula | C13H8O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
Phenalen-1-one (548-39-0)
phenalenone · perinaphthenone
Score:
#2969 in Biochemistry
,
#7269 in Chemistry
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- Phenalenone, a universal reference compound for the determination of quantum yields of singlet oxygen O2(1g) sensitization (Journal of Photochemistry and Photobiology A-chemistry, 1994)
- 1HPhenalen1one: Photophysical Properties and SingletOxygen Production (Helvetica Chimica Acta, 1991)
- Synthesis of (1S, 3aS)-8-(2,3,3a, 4,5,6-hexahydro-1H-phenalen-1-yl)-1-phenyl-1,3,8-triaza-spiro [4.5]decan-4-one, a potent and selective orphanin FQ (OFQ) receptor agonist with anxiolytic-like properties (European Journal of Medicinal Chemistry, 2000)
- Light and Singlet Oxygen in Plant Defense Against Pathogens: Phototoxic Phenalenone Phytoalexins (Accounts of Chemical Research, 2006)
- Phenalenone-type phytoalexins mediate resistance of banana plants (Musa spp.) to the burrowing nematode Radopholus similis (Proceedings of the National Academy of Sciences of the United States of America, 2014)
- Antimicrobial phenalenone derivatives from the marine-derived fungus Coniothyrium cereale (Organic and Biomolecular Chemistry, 2011)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phenalenone
- perinaphthenone
-
SMILESC1=CC2=C3C(=C1)C=CC(=O)C3=CC=C2
-
InChIKeyWWBGWPHHLRSTFI-UHFFFAOYSA-N
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Phenalen-1-one
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