| Weight | 150.206 g/mol |
|---|---|
| Formula | C7H6N2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
thieno[2,3-b]pyridin-3-amine (26763-71-3)
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- Cross-Coupling Methods for the Large-Scale Preparation of an ImidazoleThienopyridine: Synthesis of [2-(3-Methyl-3H-imidazol-4-yl)- thieno[3,2-b]pyridin-7-yl]-(2-methyl-1H-indol-5-yl)-amine (Organic Process Research & Development, 2003)
- N-(4-Chloro-phen-yl)-5-(4,5-dihydro-1H-imidazol-2-yl)thieno[2,3-b]pyridin-4-amine. (Acta Crystallographica Section E-structure Reports Online, 2012)
- Substituted 1H-pyrazolo[3,4,4,5]thieno[2,3-b]pyridin-3-amine analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M4 (2012)
- 6-Bromo-N-(6-bromo-pyridin-2-yl)-N-[4-(2,3-di-hydro-thieno[3,4-b][1,4]dioxin-5-yl)phen-yl]pyridin-2-amine. (Acta Crystallographica Section E-structure Reports Online, 2014)
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SMILESC1=CC2=C(N=C1)SC=C2N
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InChIKeyFIJSXJNXPHKJIR-UHFFFAOYSA-N
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thieno[2,3-b]pyridin-3-amine
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