Weight | 204.229 g/mol |
---|---|
Formula | C11H12N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
Ethyl 3-amino-1H-indole-2-carboxylate (87223-77-6)
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- Temperature-Gradient-Directed NMR Monitoring of a [3 + 3]-Cyclocondensation Reaction Between Alkynone and Ethyl 2-Amino-1H-indole-3-carboxylate Toward the Synthesis of Pyrimido[1,2-a]indole Catalyzed by Cs2CO3 (Synthetic Communications, 2013)
- Microwave-assisted synthesis and antibacterial activity of methyl 1-{2-[4-amino-5-(naphthalen-1-yl)-4H-1,2,4-triazol-3-ylthio]ethyl}-1H-indole-3-carboxylate derivatives (Journal of Chemical Research-s, 2013)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)C1=C(C2=CC=CC=C2N1)N
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