| Weight | 148.161 g/mol |
|---|---|
| Formula | C9H8O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
dihydrocoumarin (119-84-6)
3,4-dihydrocoumarin
Score:
#940 in Biochemistry
,
#3103 in Chemistry
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- Studies on the mechanism of Coumarin-induced toxicity in rat hepatocytes: comparison with dihydrocoumarin and other coumarin metabolites (Toxicology and Applied Pharmacology, 1989)
- Novel isocyanide-based four-component reaction: a facile synthesis of fully substituted 3,4-dihydrocoumarin derivatives. (Organic Letters, 2008)
- The Flavoring Agent Dihydrocoumarin Reverses Epigenetic Silencing and Inhibits Sirtuin Deacetylases (PLOS Genetics, 2005)
- Asymmetric synthesis of 3,4-dihydrocoumarin motif with an all-carbon quaternary stereocenter via a Michael-acetalization sequence with bifunctional amine-thiourea organocatalysts. (Organic Letters, 2011)
- 3,4Dihydrocoumarin hydrolase with haloperoxidase activity from Acinetobacter calcoaceticus F46 (FEBS Journal, 2000)
- Enantioselective synthesis of dihydrocoumarin derivatives by chiral scandium(III)-complex catalyzed inverse-electron-demand hetero-DielsAlder reaction (Chemical Communications, 2015)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,4-dihydrocoumarin
-
SMILESC1CC(=O)OC2=CC=CC=C21
-
InChIKeyVMUXSMXIQBNMGZ-UHFFFAOYSA-N
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dihydrocoumarin
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