| Weight | 175.187 g/mol |
|---|---|
| Formula | C10H9NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Methyl indole-3-carboxylate (942-24-5)
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- Nanoliposomes for encapsulation and delivery of the potential antitumoral methyl 6-methoxy-3-(4-methoxyphenyl)-1H-indole-2-carboxylate (Nanoscale Research Letters, 2011)
- Regioselective dibromination of methyl indole-3-carboxylate and application in the synthesis of 5,6-dibromoindoles. (Organic and Biomolecular Chemistry, 2011)
- Ring Contraction Reactions of Methyl Quinoline 1-Oxide 5-Carboxylates via the Corresponding Benz [d]-1, 3-oxazepines. A Facile Synthesis of Methyl Indole 4-Carboxylate and Its Derivatives (Chemical & Pharmaceutical Bulletin, 1979)
- Stereoselective synthesis of methyl 3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1-carboxylate: A key intermediate for the preparation of tacamine-type indole alkaloids (Tetrahedron Letters, 1996)
- Reaction of methyl 2,3,5,6,11,11b-hexahydro-3-oxo-1H-indolizino[8,7-b]indole-5-carboxylate and its derivatives with N-bromosuccinimide. (Bulletin of the Chemical Society of Japan, 1989)
- Alkylation par des drivs d'indole. N-Ethylation de pipridines par le mthyl-1 ethoxy-2 indole carboxylate-3 d'thyle (Journal of Heterocyclic Chemistry, 1975)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)C1=CNC2=CC=CC=C21
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InChIKeyQXAUTQFAWKKNLM-UHFFFAOYSA-N
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