| Weight | 120.151 g/mol |
|---|---|
| Formula | C8H8O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,3-DIHYDROBENZOFURAN (496-16-2)
coumaran
Score:
#2476 in Biochemistry
,
#6183 in Chemistry
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- Metabolism of 2,2-dimethyl-2,3-dihydrobenzofuran-7-N-methylcarbamate (Furadan) in plants, insects, and mamals (Journal of Agricultural and Food Chemistry, 1968)
- Dihydrobenzofuran Analogues of Hallucinogens. 3.1 Models of 4-Substituted (2,5-Dimethoxyphenyl)alkylamine Derivatives with Rigidified Methoxy Groups2 (Journal of Medicinal Chemistry, 1996)
- Stereoselective syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogues (Bioorganic & Medicinal Chemistry, 1996)
- Hydrodeoxygenation of benzofuran and its oxygenated derivatives (2,3-dihydrobenzofuran and 2-ethylphenol) over NiMoP/Al2O3 catalyst (Applied Catalysis A-general, 2009)
- Application of Huisgen (3 + 2) cycloaddition reaction: Synthesis of 1-(2,3-dihydrobenzofuran-2-yl-methyl [1,2,3]-triazoles and their antitubercular evaluations (European Journal of Medicinal Chemistry, 2010)
- Novel 2,3-Dihydrobenzofuran-2-carboxylic Acids: Highly Potent and Subtype-Selective PPAR Agonists with Potent Hypolipidemic Activity (Journal of Medicinal Chemistry, 2005)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - coumaran
-
SMILESC1COC2=CC=CC=C21
-
InChIKeyHBEDSQVIWPRPAY-UHFFFAOYSA-N
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2,3-DIHYDROBENZOFURAN
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