| Weight | 175.187 g/mol |
|---|---|
| Formula | C10H9NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Methyl 1H-indole-2-carboxylate (1202-04-6)
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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)
- Robust Synthesis of Methyl 5-Chloro-4-fluoro-1H-indole-2-carboxylate: A Key Intermediate in the Preparation of an HIV NNRTI Candidate (Organic Process Research & Development, 2010)
- 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)
- Five-membred 2,3-dioxoheterocycles: LXXXI. Reactions of 4,5-bis(methoxycarbonyl)-1H-pyrrole-2,3-diones with N-substituted 3-amino-5,5-dimethyl-2-cyclohex-2-en-1-ones. crystal and molecular structure of methyl 4-hydroxy-6,6-dimethyl-1,1-bis(4-methylphenyl)-2,4,5-trioxo-1,1,2,4,5,5,6,7-octahydrospiro[indole-3,2-pyrrole]-3-carboxylate (Russian Journal of Organic Chemistry, 2011)
- Spectroscopic (FT-IR, FT-Raman, UV, 1H and 13C NMR) profiling and computational studies on methyl 5-methoxy-1H-indole-2-carboxylate: A potential precursor to biologically active molecules (Journal of Molecular Structure, 2017)
- Structural Analogs of Umifenovir. 1. Synthesis and Biological Activity of Ethyl 5-Hydroxy-1-Methyl-2-(Trans-2-Phenylcyclopropyl)-1H-Indole-3-Carboxylate (Chemistry of Heterocyclic Compounds, 2014)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCOC(=O)C1=CC2=CC=CC=C2N1
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InChIKeyNQPIEWBAWBFGOB-UHFFFAOYSA-N
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Methyl 1H-indole-2-carboxylate
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