| Weight | 132.166 g/mol |
|---|---|
| Formula | C8H8N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
6-Aminoindole (5318-27-4)
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- New 5H-1,2,4-triazino[5,6-b]indole and aminoindole derivatives. Synthesis and studies as inhibitors of blood platelet aggregation, anti-hypertensive agents and thromboxane synthetase inhibitors (European Journal of Medicinal Chemistry, 1991)
- SONICATION AND ALUMINUM AMALGAM IN THE LEIMGRUBER-BATCHO REACTION. AN IMPROVED PREPARATION OF 6-AMINOINDOLE (Organic Preparations and Procedures International, 1995)
- Synthesis of N-Aminoindole Ureas from Ethyl 1-Amino-6-(trifluoromethyl)-1H-indole-3-carboxylate (Synlett, 2001)
- Ring Closure Reactions of 2,6-Diazaheptatrienyl Metal Compounds: Synthesis of 3-Aminoindole Derivatives and 14-Membered Macrocyclic Dimers (Journal of Organic Chemistry, 2011)
- Electrochemical nanogravimetric study of the electropolymerization of 6-aminoindole and the redox transformations of the polymer formed in aqueous media (Journal of Solid State Electrochemistry, 2013)
- Synthesis of pyrroloquinolines from 2,3-dimethyl-5-methoxy-6-aminoindole (Chemistry of Heterocyclic Compounds, 1997)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC2=C1C=CN2)N
-
InChIKeyMIMYTSWNVBMNRH-UHFFFAOYSA-N
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