| Weight | 177.203 g/mol |
|---|---|
| Formula | C10H11NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
4,7-dimethoxy-1H-indole (23876-39-3)
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- Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment. 5. An evolution from indole to azaindoles leading to the discovery of 1-(4-benzoylpiperazin-1-yl)-2-(4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)ethane-1,2-dione (BMS-488043), a drug candidate that demonstrates antiviral activity in HIV-1-infected subjects. (Journal of Medicinal Chemistry, 2009)
- Synthesis and demethylation of new 5,6,7,8-tetrahydro-4,9-dimethoxy-1H-benz[f]indole (Journal of Heterocyclic Chemistry, 1982)
- AN IMPROVED SYNTHESIS OF 4,7-DIMETHOXY-1H-INDOLE (Organic Preparations and Procedures International, 1992)
- ChemInform Abstract: Synthesis and Demethylation of New 5,6,7,8-Tetrahydro-4,9-dimethoxy-1H-benz[f]indole. (ChemInform, 1983)
- ChemInform Abstract: An Improved Synthesis of 4,7-Dimethoxy-1H-indole. (ChemInform, 2010)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=C2C=CNC2=C(C=C1)OC
-
InChIKeyOUDGAYDZZUTPPC-UHFFFAOYSA-N
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